Canonical Allele Identifier: CA038265
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 1147953
ClinVar RCV Id: RCV001487670
dbSNP Id: rs768466575

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120420C>T , CM000681.2:g.11120420C>T GRCh38
NC_000019.9:g.11231096C>T , CM000681.1:g.11231096C>T GRCh37
NC_000019.8:g.11092096C>T NCBI36
NG_009060.1:g.36040C>T , LRG_274:g.36040C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2296C>T ENSP00000252444.6:p.Leu766=
ENST00000559340.2:c.*107C>T ENSP00000453696.2:n.*107C>T
ENST00000560467.2:c.1918C>T ENSP00000453513.2:p.Leu640=
ENST00000558518.6:c.2038C>T MANE Select ENSP00000454071.1:p.Leu680=
ENST00000252444.9:c.2292C>T
ENST00000455727.6:c.1534C>T ENSP00000397829.2:p.Leu512=
ENST00000535915.5:c.1915C>T ENSP00000440520.1:p.Leu639=
ENST00000545707.5:c.1606+187C>T ENSP00000437639.1:n.1606+187C>T
ENST00000557933.5:c.2038C>T ENSP00000453557.1:p.Leu680=
ENST00000558013.5:c.2038C>T ENSP00000453346.1:p.Leu680=
ENST00000558518.5:c.2038C>T ENSP00000454071.1:p.Leu680=
NM_000527.4:c.2038C>T , LRG_274t1:c.2038C>T NP_000518.1:p.Leu680=
NM_001195798.1:c.2038C>T NP_001182727.1:p.Leu680=
NM_001195799.1:c.1915C>T NP_001182728.1:p.Leu639=
NM_001195800.1:c.1534C>T NP_001182729.1:p.Leu512=
NM_001195803.1:c.1606+187C>T NP_001182732.1:n.1606+187C>T
XM_011528010.1:c.2038C>T XP_011526312.1:p.Leu680=
XM_011528011.1:c.1657C>T XP_011526313.1:p.Leu553=
XR_244074.2:n.2048C>T
XM_011528010.2:c.2038C>T XP_011526312.1:p.Leu680=
XR_001753685.2:n.2155C>T
XR_001753686.2:n.2015C>T
NM_000527.5:c.2038C>T MANE Select NP_000518.1:p.Leu680=
NM_001195798.2:c.2038C>T NP_001182727.1:p.Leu680=
NM_001195799.2:c.1915C>T NP_001182728.1:p.Leu639=
NM_001195800.2:c.1534C>T NP_001182729.1:p.Leu512=
NM_001195803.2:c.1606+187C>T NP_001182732.1:n.1606+187C>T