Canonical Allele Identifier: CA032264
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 891661
ClinVar RCV Id: RCV001127091
dbSNP Id: rs756672317

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11111613C>T , CM000681.2:g.11111613C>T GRCh38
NC_000019.9:g.11222289C>T , CM000681.1:g.11222289C>T GRCh37
NC_000019.8:g.11083289C>T NCBI36
NG_009060.1:g.27233C>T , LRG_274:g.27233C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.1418C>T ENSP00000252444.6:p.Pro473Leu
ENST00000559340.2:c.1160C>T ENSP00000453696.2:p.Pro387Leu
ENST00000560467.2:c.1040C>T ENSP00000453513.2:p.Pro347Leu
ENST00000558518.6:c.1160C>T MANE Select ENSP00000454071.1:p.Pro387Leu
ENST00000252444.9:c.1414C>T
ENST00000455727.6:c.656C>T ENSP00000397829.2:p.Pro219Leu
ENST00000535915.5:c.1037C>T ENSP00000440520.1:p.Pro346Leu
ENST00000545707.5:c.779C>T ENSP00000437639.1:p.Pro260Leu
ENST00000557933.5:c.1160C>T ENSP00000453557.1:p.Pro387Leu
ENST00000558013.5:c.1160C>T ENSP00000453346.1:p.Pro387Leu
ENST00000558518.5:c.1160C>T ENSP00000454071.1:p.Pro387Leu
ENST00000560173.1:n.159C>T
ENST00000560467.1:c.640C>T
NM_000527.4:c.1160C>T , LRG_274t1:c.1160C>T NP_000518.1:p.Pro387Leu
NM_001195798.1:c.1160C>T NP_001182727.1:p.Pro387Leu
NM_001195799.1:c.1037C>T NP_001182728.1:p.Pro346Leu
NM_001195800.1:c.656C>T NP_001182729.1:p.Pro219Leu
NM_001195803.1:c.779C>T NP_001182732.1:p.Pro260Leu
XM_011528010.1:c.1160C>T XP_011526312.1:p.Pro387Leu
XM_011528011.1:c.779C>T XP_011526313.1:p.Pro260Leu
XR_244074.2:n.1310C>T
XM_011528010.2:c.1160C>T XP_011526312.1:p.Pro387Leu
XR_001753685.2:n.1277C>T
XR_001753686.2:n.1277C>T
NM_000527.5:c.1160C>T MANE Select NP_000518.1:p.Pro387Leu
NM_001195798.2:c.1160C>T NP_001182727.1:p.Pro387Leu
NM_001195799.2:c.1037C>T NP_001182728.1:p.Pro346Leu
NM_001195800.2:c.656C>T NP_001182729.1:p.Pro219Leu
NM_001195803.2:c.779C>T NP_001182732.1:p.Pro260Leu