Canonical Allele Identifier: CA2830534974
Gene: BLTP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.122254984_122254985insTTAAAG , CM000666.2:g.122254984_122254985insTTAAAG GRCh38
NC_000004.11:g.123176139_123176140insTTAAAG , CM000666.1:g.123176139_123176140insTTAAAG GRCh37
NC_000004.10:g.123395589_123395590insTTAAAG NCBI36
NG_015813.1:g.89382_89383insTTAAAG
NG_015813.2:g.89382_89383insTTAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000388738.8:c.6225+29_6225+30insTTAAAG ENSP00000373390.4:n.6225+29_6225+30insTTAAAG
ENST00000684987.1:n.6548+29_6548+30insTTAAAG
ENST00000686075.1:n.6548+29_6548+30insTTAAAG
ENST00000690536.1:n.6548+29_6548+30insTTAAAG
ENST00000693334.1:n.6548+29_6548+30insTTAAAG
ENST00000693420.1:c.6225+29_6225+30insTTAAAG ENSP00000509435.1:n.6225+29_6225+30insTTAAAG
ENST00000679879.1:c.6225+29_6225+30insTTAAAG MANE Select ENSP00000505357.1:n.6225+29_6225+30insTTAAAG
ENST00000264501.8:c.6225+29_6225+30insTTAAAG ENSP00000264501.4:n.6225+29_6225+30insTTAAAG
ENST00000388738.7:c.6225+29_6225+30insTTAAAG ENSP00000373390.3:n.6225+29_6225+30insTTAAAG
ENST00000419325.5:c.97+29_97+30insTTAAAG
ENST00000446180.5:c.1943+29_1943+30insTTAAAG
NM_015312.3:c.6225+29_6225+30insTTAAAG NP_056127.2:n.6225+29_6225+30insTTAAAG
XM_005263282.1:c.6225+29_6225+30insTTAAAG XP_005263339.1:n.6225+29_6225+30insTTAAAG
XM_005263287.1:c.6225+29_6225+30insTTAAAG XP_005263344.1:n.6225+29_6225+30insTTAAAG
XM_006714343.1:c.6225+29_6225+30insTTAAAG XP_006714406.1:n.6225+29_6225+30insTTAAAG
XM_006714344.1:c.6222+29_6222+30insTTAAAG XP_006714407.1:n.6222+29_6222+30insTTAAAG
XM_011532319.1:c.6225+29_6225+30insTTAAAG XP_011530621.1:n.6225+29_6225+30insTTAAAG
XM_011532320.1:c.6225+29_6225+30insTTAAAG XP_011530622.1:n.6225+29_6225+30insTTAAAG
XM_011532321.1:c.6225+29_6225+30insTTAAAG XP_011530623.1:n.6225+29_6225+30insTTAAAG
XM_011532322.1:c.6222+29_6222+30insTTAAAG XP_011530624.1:n.6222+29_6222+30insTTAAAG
XM_011532323.1:c.6225+29_6225+30insTTAAAG XP_011530625.1:n.6225+29_6225+30insTTAAAG
XM_011532324.1:c.6225+29_6225+30insTTAAAG XP_011530626.1:n.6225+29_6225+30insTTAAAG
XM_011532325.1:c.6225+29_6225+30insTTAAAG XP_011530627.1:n.6225+29_6225+30insTTAAAG
XM_011532326.1:c.6096+29_6096+30insTTAAAG XP_011530628.1:n.6096+29_6096+30insTTAAAG
XM_011532327.1:c.6075+29_6075+30insTTAAAG XP_011530629.1:n.6075+29_6075+30insTTAAAG
XM_011532328.1:c.6225+29_6225+30insTTAAAG XP_011530630.1:n.6225+29_6225+30insTTAAAG
XM_011532329.1:c.6225+29_6225+30insTTAAAG XP_011530631.1:n.6225+29_6225+30insTTAAAG
XM_011532330.1:c.4476+29_4476+30insTTAAAG XP_011530632.1:n.4476+29_4476+30insTTAAAG
XM_011532331.1:c.6225+29_6225+30insTTAAAG XP_011530633.1:n.6225+29_6225+30insTTAAAG
XR_938781.1:n.6598+29_6598+30insTTAAAG
XR_938782.1:n.6598+29_6598+30insTTAAAG
XR_938783.1:n.6598+29_6598+30insTTAAAG
XM_011532320.3:c.6225+29_6225+30insTTAAAG XP_011530622.1:n.6225+29_6225+30insTTAAAG
XM_011532321.2:c.6225+29_6225+30insTTAAAG XP_011530623.1:n.6225+29_6225+30insTTAAAG
XM_017008695.1:c.6225+29_6225+30insTTAAAG XP_016864184.1:n.6225+29_6225+30insTTAAAG
XM_017008696.1:c.6225+29_6225+30insTTAAAG XP_016864185.1:n.6225+29_6225+30insTTAAAG
XM_017008697.1:c.6225+29_6225+30insTTAAAG XP_016864186.1:n.6225+29_6225+30insTTAAAG
XM_017008698.1:c.3456+29_3456+30insTTAAAG XP_016864187.1:n.3456+29_3456+30insTTAAAG
XM_017008699.1:c.6225+29_6225+30insTTAAAG XP_016864188.1:n.6225+29_6225+30insTTAAAG
XM_024454243.1:c.4377+29_4377+30insTTAAAG XP_024310011.1:n.4377+29_4377+30insTTAAAG
XR_001741335.2:n.6598+29_6598+30insTTAAAG
XR_001741336.1:n.6598+29_6598+30insTTAAAG
XR_001741337.1:n.6598+29_6598+30insTTAAAG
NM_001384125.1:c.6225+29_6225+30insTTAAAG MANE Select NP_001371054.1:n.6225+29_6225+30insTTAAAG
NM_015312.4:c.6225+29_6225+30insTTAAAG NP_056127.2:n.6225+29_6225+30insTTAAAG