Canonical Allele Identifier: CA783244182
Gene: LDLR HGNC NCBI

Linked Data

dbSNP Id: rs1216601175

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11114830_11114831insA , CM000681.2:g.11114830_11114831insA GRCh38
NC_000019.9:g.11225506_11225507insA , CM000681.1:g.11225506_11225507insA GRCh37
NC_000019.8:g.11086506_11086507insA NCBI36
NG_009060.1:g.30450_30451insA , LRG_274:g.30450_30451insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1844+1068_1844+1069insA ENSP00000252444.6:n.1844+1068_1844+1069insA
ENST00000559340.2:c.1586+1068_1586+1069insA ENSP00000453696.2:n.1586+1068_1586+1069insA
ENST00000560467.2:c.1466+1068_1466+1069insA ENSP00000453513.2:n.1466+1068_1466+1069insA
ENST00000558518.6:c.1586+1068_1586+1069insA MANE Select ENSP00000454071.1:n.1586+1068_1586+1069insA
ENST00000252444.9:c.1840+1068_1840+1069insA
ENST00000455727.6:c.1082+1068_1082+1069insA ENSP00000397829.2:n.1082+1068_1082+1069insA
ENST00000535915.5:c.1463+1068_1463+1069insA ENSP00000440520.1:n.1463+1068_1463+1069insA
ENST00000545707.5:c.1205+1068_1205+1069insA ENSP00000437639.1:n.1205+1068_1205+1069insA
ENST00000557933.5:c.1586+1068_1586+1069insA ENSP00000453557.1:n.1586+1068_1586+1069insA
ENST00000558013.5:c.1586+1068_1586+1069insA ENSP00000453346.1:n.1586+1068_1586+1069insA
ENST00000558518.5:c.1586+1068_1586+1069insA ENSP00000454071.1:n.1586+1068_1586+1069insA
ENST00000559340.1:c.307+1068_307+1069insA
NM_000527.4:c.1586+1068_1586+1069insA , LRG_274t1:c.1586+1068_1586+1069insA NP_000518.1:n.1586+1068_1586+1069insA
NM_001195798.1:c.1586+1068_1586+1069insA NP_001182727.1:n.1586+1068_1586+1069insA
NM_001195799.1:c.1463+1068_1463+1069insA NP_001182728.1:n.1463+1068_1463+1069insA
NM_001195800.1:c.1082+1068_1082+1069insA NP_001182729.1:n.1082+1068_1082+1069insA
NM_001195803.1:c.1205+1068_1205+1069insA NP_001182732.1:n.1205+1068_1205+1069insA
XM_011528010.1:c.1586+1068_1586+1069insA XP_011526312.1:n.1586+1068_1586+1069insA
XM_011528011.1:c.1205+1068_1205+1069insA XP_011526313.1:n.1205+1068_1205+1069insA
XR_244074.2:n.1736+1068_1736+1069insA
XM_011528010.2:c.1586+1068_1586+1069insA XP_011526312.1:n.1586+1068_1586+1069insA
XR_001753685.2:n.1703+1068_1703+1069insA
XR_001753686.2:n.1703+1068_1703+1069insA
NM_000527.5:c.1586+1068_1586+1069insA MANE Select NP_000518.1:n.1586+1068_1586+1069insA
NM_001195798.2:c.1586+1068_1586+1069insA NP_001182727.1:n.1586+1068_1586+1069insA
NM_001195799.2:c.1463+1068_1463+1069insA NP_001182728.1:n.1463+1068_1463+1069insA
NM_001195800.2:c.1082+1068_1082+1069insA NP_001182729.1:n.1082+1068_1082+1069insA
NM_001195803.2:c.1205+1068_1205+1069insA NP_001182732.1:n.1205+1068_1205+1069insA