Canonical Allele Identifier: CA2322770792
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111634_11111635delinsCT , CM000681.2:g.11111634_11111635delinsCT GRCh38
NC_000019.9:g.11222310_11222311delinsCT , CM000681.1:g.11222310_11222311delinsCT GRCh37
NC_000019.8:g.11083310_11083311delinsCT NCBI36
NG_009060.1:g.27254_27255delinsCT , LRG_274:g.27254_27255delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1439_1440delinsCT ENSP00000252444.6:p.Ala480=
ENST00000559340.2:c.1181_1182delinsCT ENSP00000453696.2:p.Ala394=
ENST00000560467.2:c.1061_1062delinsCT ENSP00000453513.2:p.Ala354=
ENST00000558518.6:c.1181_1182delinsCT MANE Select ENSP00000454071.1:p.Ala394=
ENST00000252444.9:c.1435_1436delinsCT
ENST00000455727.6:c.677_678delinsCT ENSP00000397829.2:p.Ala226=
ENST00000535915.5:c.1058_1059delinsCT ENSP00000440520.1:p.Ala353=
ENST00000545707.5:c.800_801delinsCT ENSP00000437639.1:p.Ala267=
ENST00000557933.5:c.1181_1182delinsCT ENSP00000453557.1:p.Ala394=
ENST00000558013.5:c.1181_1182delinsCT ENSP00000453346.1:p.Ala394=
ENST00000558518.5:c.1181_1182delinsCT ENSP00000454071.1:p.Ala394=
ENST00000560173.1:n.180_181delinsCT
ENST00000560467.1:c.661_662delinsCT
NM_000527.4:c.1181_1182delinsCT , LRG_274t1:c.1181_1182delinsCT NP_000518.1:p.Ala394=
NM_001195798.1:c.1181_1182delinsCT NP_001182727.1:p.Ala394=
NM_001195799.1:c.1058_1059delinsCT NP_001182728.1:p.Ala353=
NM_001195800.1:c.677_678delinsCT NP_001182729.1:p.Ala226=
NM_001195803.1:c.800_801delinsCT NP_001182732.1:p.Ala267=
XM_011528010.1:c.1181_1182delinsCT XP_011526312.1:p.Ala394=
XM_011528011.1:c.800_801delinsCT XP_011526313.1:p.Ala267=
XR_244074.2:n.1331_1332delinsCT
XM_011528010.2:c.1181_1182delinsCT XP_011526312.1:p.Ala394=
XR_001753685.2:n.1298_1299delinsCT
XR_001753686.2:n.1298_1299delinsCT
NM_000527.5:c.1181_1182delinsCT MANE Select NP_000518.1:p.Ala394=
NM_001195798.2:c.1181_1182delinsCT NP_001182727.1:p.Ala394=
NM_001195799.2:c.1058_1059delinsCT NP_001182728.1:p.Ala353=
NM_001195800.2:c.677_678delinsCT NP_001182729.1:p.Ala226=
NM_001195803.2:c.800_801delinsCT NP_001182732.1:p.Ala267=