Canonical Allele Identifier: CA404093158
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11120200A>C , CM000681.2:g.11120200A>C GRCh38
NC_000019.9:g.11230876A>C , CM000681.1:g.11230876A>C GRCh37
NC_000019.8:g.11091876A>C NCBI36
NG_009060.1:g.35820A>C , LRG_274:g.35820A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2212A>C ENSP00000252444.6:p.Met738Leu
ENST00000559340.2:c.*23A>C ENSP00000453696.2:n.*23A>C
ENST00000560467.2:c.1834A>C ENSP00000453513.2:p.Met612Leu
ENST00000558518.6:c.1954A>C MANE Select ENSP00000454071.1:p.Met652Leu
ENST00000252444.9:c.2208A>C
ENST00000455727.6:c.1450A>C ENSP00000397829.2:p.Met484Leu
ENST00000535915.5:c.1831A>C ENSP00000440520.1:p.Met611Leu
ENST00000545707.5:c.1573A>C ENSP00000437639.1:p.Met525Leu
ENST00000557933.5:c.1954A>C ENSP00000453557.1:p.Met652Leu
ENST00000558013.5:c.1954A>C ENSP00000453346.1:p.Met652Leu
ENST00000558518.5:c.1954A>C ENSP00000454071.1:p.Met652Leu
ENST00000559340.1:c.535A>C
NM_000527.4:c.1954A>C , LRG_274t1:c.1954A>C NP_000518.1:p.Met652Leu
NM_001195798.1:c.1954A>C NP_001182727.1:p.Met652Leu
NM_001195799.1:c.1831A>C NP_001182728.1:p.Met611Leu
NM_001195800.1:c.1450A>C NP_001182729.1:p.Met484Leu
NM_001195803.1:c.1573A>C NP_001182732.1:p.Met525Leu
XM_011528010.1:c.1954A>C XP_011526312.1:p.Met652Leu
XM_011528011.1:c.1573A>C XP_011526313.1:p.Met525Leu
XR_244074.2:n.1964A>C
XM_011528010.2:c.1954A>C XP_011526312.1:p.Met652Leu
XR_001753685.2:n.2071A>C
XR_001753686.2:n.1931A>C
NM_000527.5:c.1954A>C MANE Select NP_000518.1:p.Met652Leu
NM_001195798.2:c.1954A>C NP_001182727.1:p.Met652Leu
NM_001195799.2:c.1831A>C NP_001182728.1:p.Met611Leu
NM_001195800.2:c.1450A>C NP_001182729.1:p.Met484Leu
NM_001195803.2:c.1573A>C NP_001182732.1:p.Met525Leu