Canonical Allele Identifier: CA2322771644
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11113231T= , CM000681.2:g.11113231T= GRCh38
NC_000019.9:g.11223907T= , CM000681.1:g.11223907T= GRCh37
NC_000019.8:g.11084907T= NCBI36
NG_009060.1:g.28851T= , LRG_274:g.28851T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1445-47T= ENSP00000252444.6:n.1445-47T=
ENST00000559340.2:c.1187-47T= ENSP00000453696.2:n.1187-47T=
ENST00000560467.2:c.1067-47T= ENSP00000453513.2:n.1067-47T=
ENST00000558518.6:c.1187-47T= MANE Select ENSP00000454071.1:n.1187-47T=
ENST00000252444.9:c.1441-47T=
ENST00000455727.6:c.683-47T= ENSP00000397829.2:n.683-47T=
ENST00000535915.5:c.1064-47T= ENSP00000440520.1:n.1064-47T=
ENST00000545707.5:c.806-47T= ENSP00000437639.1:n.806-47T=
ENST00000557933.5:c.1187-47T= ENSP00000453557.1:n.1187-47T=
ENST00000558013.5:c.1187-47T= ENSP00000453346.1:n.1187-47T=
ENST00000558518.5:c.1187-47T= ENSP00000454071.1:n.1187-47T=
ENST00000560173.1:n.186-47T=
ENST00000560467.1:c.667-47T=
NM_000527.4:c.1187-47T= , LRG_274t1:c.1187-47T= NP_000518.1:n.1187-47T=
NM_001195798.1:c.1187-47T= NP_001182727.1:n.1187-47T=
NM_001195799.1:c.1064-47T= NP_001182728.1:n.1064-47T=
NM_001195800.1:c.683-47T= NP_001182729.1:n.683-47T=
NM_001195803.1:c.806-47T= NP_001182732.1:n.806-47T=
XM_011528010.1:c.1187-47T= XP_011526312.1:n.1187-47T=
XM_011528011.1:c.806-47T= XP_011526313.1:n.806-47T=
XR_244074.2:n.1337-47T=
XM_011528010.2:c.1187-47T= XP_011526312.1:n.1187-47T=
XR_001753685.2:n.1304-47T=
XR_001753686.2:n.1304-47T=
NM_000527.5:c.1187-47T= MANE Select NP_000518.1:n.1187-47T=
NM_001195798.2:c.1187-47T= NP_001182727.1:n.1187-47T=
NM_001195799.2:c.1064-47T= NP_001182728.1:n.1064-47T=
NM_001195800.2:c.683-47T= NP_001182729.1:n.683-47T=
NM_001195803.2:c.806-47T= NP_001182732.1:n.806-47T=