Canonical Allele Identifier: CA2322779419
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11127837C= , CM000681.2:g.11127837C= GRCh38
NC_000019.9:g.11238513C= , CM000681.1:g.11238513C= GRCh37
NC_000019.8:g.11099513C= NCBI36
NG_009060.1:g.43457C= , LRG_274:g.43457C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2570-171C= ENSP00000252444.6:n.2570-171C=
ENST00000559340.2:c.*381-171C= ENSP00000453696.2:n.*381-171C=
ENST00000560467.2:c.2192-171C= ENSP00000453513.2:n.2192-171C=
ENST00000558518.6:c.2312-171C= MANE Select ENSP00000454071.1:n.2312-171C=
ENST00000252444.9:c.2566-171C=
ENST00000455727.6:c.1808-171C= ENSP00000397829.2:n.1808-171C=
ENST00000535915.5:c.2189-171C= ENSP00000440520.1:n.2189-171C=
ENST00000545707.5:c.1778-171C= ENSP00000437639.1:n.1778-171C=
ENST00000557933.5:c.2312-171C= ENSP00000453557.1:n.2312-171C=
ENST00000558013.5:c.2312-171C= ENSP00000453346.1:n.2312-171C=
ENST00000558518.5:c.2312-171C= ENSP00000454071.1:n.2312-171C=
ENST00000560628.1:n.108+183C=
NM_000527.4:c.2312-171C= , LRG_274t1:c.2312-171C= NP_000518.1:n.2312-171C=
NM_001195798.1:c.2312-171C= NP_001182727.1:n.2312-171C=
NM_001195799.1:c.2189-171C= NP_001182728.1:n.2189-171C=
NM_001195800.1:c.1808-171C= NP_001182729.1:n.1808-171C=
NM_001195803.1:c.1778-171C= NP_001182732.1:n.1778-171C=
XM_011528010.1:c.2312-1676C= XP_011526312.1:n.2312-1676C=
XM_011528011.1:c.1931-171C= XP_011526313.1:n.1931-171C=
XR_244074.2:n.2322-171C=
XM_011528010.2:c.2312-1676C= XP_011526312.1:n.2312-1676C=
XR_001753685.2:n.2646-171C=
XR_001753686.2:n.2289-171C=
NM_000527.5:c.2312-171C= MANE Select NP_000518.1:n.2312-171C=
NM_001195798.2:c.2312-171C= NP_001182727.1:n.2312-171C=
NM_001195799.2:c.2189-171C= NP_001182728.1:n.2189-171C=
NM_001195800.2:c.1808-171C= NP_001182729.1:n.1808-171C=
NM_001195803.2:c.1778-171C= NP_001182732.1:n.1778-171C=