Canonical Allele Identifier: CA2322771872
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113535C= , CM000681.2:g.11113535C= GRCh38
NC_000019.9:g.11224211C= , CM000681.1:g.11224211C= GRCh37
NC_000019.8:g.11085211C= NCBI36
NG_009060.1:g.29155C= , LRG_274:g.29155C=

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1617C= ENSP00000252444.6:p.Ser539=
ENST00000559340.2:c.1359C= ENSP00000453696.2:p.Ser453=
ENST00000560467.2:c.1239C= ENSP00000453513.2:p.Ser413=
ENST00000558518.6:c.1359C= MANE Select ENSP00000454071.1:p.Ser453=
ENST00000252444.9:c.1613C=
ENST00000455727.6:c.855C= ENSP00000397829.2:p.Ser285=
ENST00000535915.5:c.1236C= ENSP00000440520.1:p.Ser412=
ENST00000545707.5:c.978C= ENSP00000437639.1:p.Ser326=
ENST00000557933.5:c.1359C= ENSP00000453557.1:p.Ser453=
ENST00000558013.5:c.1359C= ENSP00000453346.1:p.Ser453=
ENST00000558518.5:c.1359C= ENSP00000454071.1:p.Ser453=
ENST00000559340.1:c.80C=
ENST00000560467.1:c.839C=
NM_000527.4:c.1359C= , LRG_274t1:c.1359C= NP_000518.1:p.Ser453=
NM_001195798.1:c.1359C= NP_001182727.1:p.Ser453=
NM_001195799.1:c.1236C= NP_001182728.1:p.Ser412=
NM_001195800.1:c.855C= NP_001182729.1:p.Ser285=
NM_001195803.1:c.978C= NP_001182732.1:p.Ser326=
XM_011528010.1:c.1359C= XP_011526312.1:p.Ser453=
XM_011528011.1:c.978C= XP_011526313.1:p.Ser326=
XR_244074.2:n.1509C=
XM_011528010.2:c.1359C= XP_011526312.1:p.Ser453=
XR_001753685.2:n.1476C=
XR_001753686.2:n.1476C=
NM_000527.5:c.1359C= MANE Select NP_000518.1:p.Ser453=
NM_001195798.2:c.1359C= NP_001182727.1:p.Ser453=
NM_001195799.2:c.1236C= NP_001182728.1:p.Ser412=
NM_001195800.2:c.855C= NP_001182729.1:p.Ser285=
NM_001195803.2:c.978C= NP_001182732.1:p.Ser326=