Canonical Allele Identifier: CA2322775698
Gene: LDLR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120593C= , CM000681.2:g.11120593C= GRCh38
NC_000019.9:g.11231269C= , CM000681.1:g.11231269C= GRCh37
NC_000019.8:g.11092269C= NCBI36
NG_009060.1:g.36213C= , LRG_274:g.36213C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2398+71C= ENSP00000252444.6:n.2398+71C=
ENST00000559340.2:c.*209+71C= ENSP00000453696.2:n.*209+71C=
ENST00000560467.2:c.2020+71C= ENSP00000453513.2:n.2020+71C=
ENST00000558518.6:c.2140+71C= MANE Select ENSP00000454071.1:n.2140+71C=
ENST00000252444.9:c.2394+71C=
ENST00000455727.6:c.1636+71C= ENSP00000397829.2:n.1636+71C=
ENST00000535915.5:c.2017+71C= ENSP00000440520.1:n.2017+71C=
ENST00000545707.5:c.1606+360C= ENSP00000437639.1:n.1606+360C=
ENST00000557933.5:c.2140+71C= ENSP00000453557.1:n.2140+71C=
ENST00000558013.5:c.2140+71C= ENSP00000453346.1:n.2140+71C=
ENST00000558518.5:c.2140+71C= ENSP00000454071.1:n.2140+71C=
NM_000527.4:c.2140+71C= , LRG_274t1:c.2140+71C= NP_000518.1:n.2140+71C=
NM_001195798.1:c.2140+71C= NP_001182727.1:n.2140+71C=
NM_001195799.1:c.2017+71C= NP_001182728.1:n.2017+71C=
NM_001195800.1:c.1636+71C= NP_001182729.1:n.1636+71C=
NM_001195803.1:c.1606+360C= NP_001182732.1:n.1606+360C=
XM_011528010.1:c.2140+71C= XP_011526312.1:n.2140+71C=
XM_011528011.1:c.1759+71C= XP_011526313.1:n.1759+71C=
XR_244074.2:n.2150+71C=
XM_011528010.2:c.2140+71C= XP_011526312.1:n.2140+71C=
XR_001753685.2:n.2328C=
XR_001753686.2:n.2117+71C=
NM_000527.5:c.2140+71C= MANE Select NP_000518.1:n.2140+71C=
NM_001195798.2:c.2140+71C= NP_001182727.1:n.2140+71C=
NM_001195799.2:c.2017+71C= NP_001182728.1:n.2017+71C=
NM_001195800.2:c.1636+71C= NP_001182729.1:n.1636+71C=
NM_001195803.2:c.1606+360C= NP_001182732.1:n.1606+360C=