Canonical Allele Identifier: CA404095809
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123334G>C , CM000681.2:g.11123334G>C GRCh38
NC_000019.9:g.11234010G>C , CM000681.1:g.11234010G>C GRCh37
NC_000019.8:g.11095010G>C NCBI36
NG_009060.1:g.38954G>C , LRG_274:g.38954G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2559G>C ENSP00000252444.6:p.Met853Ile
ENST00000559340.2:c.*370G>C ENSP00000453696.2:n.*370G>C
ENST00000560467.2:c.2181G>C ENSP00000453513.2:p.Met727Ile
ENST00000558518.6:c.2301G>C MANE Select ENSP00000454071.1:p.Met767Ile
ENST00000252444.9:c.2555G>C
ENST00000455727.6:c.1797G>C ENSP00000397829.2:p.Met599Ile
ENST00000535915.5:c.2178G>C ENSP00000440520.1:p.Met726Ile
ENST00000545707.5:c.1767G>C ENSP00000437639.1:p.Met589Ile
ENST00000557933.5:c.2301G>C ENSP00000453557.1:p.Met767Ile
ENST00000558013.5:c.2301G>C ENSP00000453346.1:p.Met767Ile
ENST00000558518.5:c.2301G>C ENSP00000454071.1:p.Met767Ile
NM_000527.4:c.2301G>C , LRG_274t1:c.2301G>C NP_000518.1:p.Met767Ile
NM_001195798.1:c.2301G>C NP_001182727.1:p.Met767Ile
NM_001195799.1:c.2178G>C NP_001182728.1:p.Met726Ile
NM_001195800.1:c.1797G>C NP_001182729.1:p.Met599Ile
NM_001195803.1:c.1767G>C NP_001182732.1:p.Met589Ile
XM_011528010.1:c.2301G>C XP_011526312.1:p.Met767Ile
XM_011528011.1:c.1920G>C XP_011526313.1:p.Met640Ile
XR_244074.2:n.2311G>C
XM_011528010.2:c.2301G>C XP_011526312.1:p.Met767Ile
XR_001753685.2:n.2635G>C
XR_001753686.2:n.2278G>C
NM_000527.5:c.2301G>C MANE Select NP_000518.1:p.Met767Ile
NM_001195798.2:c.2301G>C NP_001182727.1:p.Met767Ile
NM_001195799.2:c.2178G>C NP_001182728.1:p.Met726Ile
NM_001195800.2:c.1797G>C NP_001182729.1:p.Met599Ile
NM_001195803.2:c.1767G>C NP_001182732.1:p.Met589Ile