Canonical Allele Identifier: CA404096685
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11128025G>C , CM000681.2:g.11128025G>C GRCh38
NC_000019.9:g.11238701G>C , CM000681.1:g.11238701G>C GRCh37
NC_000019.8:g.11099701G>C NCBI36
NG_009060.1:g.43645G>C , LRG_274:g.43645G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2587G>C ENSP00000252444.6:p.Gly863Arg
ENST00000559340.2:c.*398G>C ENSP00000453696.2:n.*398G>C
ENST00000560467.2:c.2209G>C ENSP00000453513.2:p.Gly737Arg
ENST00000558518.6:c.2329G>C MANE Select ENSP00000454071.1:p.Gly777Arg
ENST00000252444.9:c.2583G>C
ENST00000455727.6:c.1825G>C ENSP00000397829.2:p.Gly609Arg
ENST00000535915.5:c.2206G>C ENSP00000440520.1:p.Gly736Arg
ENST00000545707.5:c.1795G>C ENSP00000437639.1:p.Gly599Arg
ENST00000557933.5:c.2329G>C ENSP00000453557.1:p.Gly777Arg
ENST00000558013.5:c.2329G>C ENSP00000453346.1:p.Gly777Arg
ENST00000558518.5:c.2329G>C ENSP00000454071.1:p.Gly777Arg
ENST00000560628.1:n.108+371G>C
NM_000527.4:c.2329G>C , LRG_274t1:c.2329G>C NP_000518.1:p.Gly777Arg
NM_001195798.1:c.2329G>C NP_001182727.1:p.Gly777Arg
NM_001195799.1:c.2206G>C NP_001182728.1:p.Gly736Arg
NM_001195800.1:c.1825G>C NP_001182729.1:p.Gly609Arg
NM_001195803.1:c.1795G>C NP_001182732.1:p.Gly599Arg
XM_011528010.1:c.2312-1488G>C XP_011526312.1:n.2312-1488G>C
XM_011528011.1:c.1948G>C XP_011526313.1:p.Gly650Arg
XR_244074.2:n.2339G>C
XM_011528010.2:c.2312-1488G>C XP_011526312.1:n.2312-1488G>C
XR_001753685.2:n.2663G>C
XR_001753686.2:n.2306G>C
NM_000527.5:c.2329G>C MANE Select NP_000518.1:p.Gly777Arg
NM_001195798.2:c.2329G>C NP_001182727.1:p.Gly777Arg
NM_001195799.2:c.2206G>C NP_001182728.1:p.Gly736Arg
NM_001195800.2:c.1825G>C NP_001182729.1:p.Gly609Arg
NM_001195803.2:c.1795G>C NP_001182732.1:p.Gly599Arg