Canonical Allele Identifier: CA10585553
Gene: LDLR HGNC NCBI

Linked Data

ClinVar Variation Id: 251962
ClinVar RCV Id: RCV000238213
dbSNP Id: rs879254978

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11116171T>C , CM000681.2:g.11116171T>C GRCh38
NC_000019.9:g.11226847T>C , CM000681.1:g.11226847T>C GRCh37
NC_000019.8:g.11087847T>C NCBI36
NG_009060.1:g.31791T>C , LRG_274:g.31791T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252444.10:c.1922T>C ENSP00000252444.6:p.Leu641Pro
ENST00000559340.2:c.1664T>C ENSP00000453696.2:p.Leu555Pro
ENST00000560467.2:c.1544T>C ENSP00000453513.2:p.Leu515Pro
ENST00000558518.6:c.1664T>C MANE Select ENSP00000454071.1:p.Leu555Pro
ENST00000252444.9:c.1918T>C
ENST00000455727.6:c.1160T>C ENSP00000397829.2:p.Leu387Pro
ENST00000535915.5:c.1541T>C ENSP00000440520.1:p.Leu514Pro
ENST00000545707.5:c.1283T>C ENSP00000437639.1:p.Leu428Pro
ENST00000557933.5:c.1664T>C ENSP00000453557.1:p.Leu555Pro
ENST00000558013.5:c.1664T>C ENSP00000453346.1:p.Leu555Pro
ENST00000558518.5:c.1664T>C ENSP00000454071.1:p.Leu555Pro
ENST00000559340.1:c.385T>C
NM_000527.4:c.1664T>C , LRG_274t1:c.1664T>C NP_000518.1:p.Leu555Pro
NM_001195798.1:c.1664T>C NP_001182727.1:p.Leu555Pro
NM_001195799.1:c.1541T>C NP_001182728.1:p.Leu514Pro
NM_001195800.1:c.1160T>C NP_001182729.1:p.Leu387Pro
NM_001195803.1:c.1283T>C NP_001182732.1:p.Leu428Pro
XM_011528010.1:c.1664T>C XP_011526312.1:p.Leu555Pro
XM_011528011.1:c.1283T>C XP_011526313.1:p.Leu428Pro
XR_244074.2:n.1814T>C
XM_011528010.2:c.1664T>C XP_011526312.1:p.Leu555Pro
XR_001753685.2:n.1781T>C
XR_001753686.2:n.1781T>C
NM_000527.5:c.1664T>C MANE Select NP_000518.1:p.Leu555Pro
NM_001195798.2:c.1664T>C NP_001182727.1:p.Leu555Pro
NM_001195799.2:c.1541T>C NP_001182728.1:p.Leu514Pro
NM_001195800.2:c.1160T>C NP_001182729.1:p.Leu387Pro
NM_001195803.2:c.1283T>C NP_001182732.1:p.Leu428Pro