Canonical Allele Identifier: CA404099764
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129648A>C , CM000681.2:g.11129648A>C GRCh38
NC_000019.9:g.11240324A>C , CM000681.1:g.11240324A>C GRCh37
NC_000019.8:g.11101324A>C NCBI36
NG_009060.1:g.45268A>C , LRG_274:g.45268A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2783A>C ENSP00000252444.6:p.Gln928Pro
ENST00000559340.2:c.*594A>C ENSP00000453696.2:n.*594A>C
ENST00000560467.2:c.2405A>C ENSP00000453513.2:p.Gln802Pro
ENST00000558518.6:c.2525A>C MANE Select ENSP00000454071.1:p.Gln842Pro
ENST00000252444.9:c.2779A>C
ENST00000455727.6:c.2021A>C ENSP00000397829.2:p.Gln674Pro
ENST00000535915.5:c.2402A>C ENSP00000440520.1:p.Gln801Pro
ENST00000545707.5:c.1991A>C ENSP00000437639.1:p.Gln664Pro
ENST00000557933.5:c.2587A>C ENSP00000453557.1:p.Arg863=
ENST00000558013.5:c.2525A>C ENSP00000453346.1:p.Gln842Pro
ENST00000558518.5:c.2525A>C ENSP00000454071.1:p.Gln842Pro
ENST00000560628.1:n.108+1994A>C
NM_000527.4:c.2525A>C , LRG_274t1:c.2525A>C NP_000518.1:p.Gln842Pro
NM_001195798.1:c.2525A>C NP_001182727.1:p.Gln842Pro
NM_001195799.1:c.2402A>C NP_001182728.1:p.Gln801Pro
NM_001195800.1:c.2021A>C NP_001182729.1:p.Gln674Pro
NM_001195803.1:c.1991A>C NP_001182732.1:p.Gln664Pro
XM_011528010.1:c.2447A>C XP_011526312.1:p.Gln816Pro
XM_011528011.1:c.2144A>C XP_011526313.1:p.Gln715Pro
XM_011528010.2:c.2447A>C XP_011526312.1:p.Gln816Pro
XR_001753685.2:n.2859A>C
XR_001753686.2:n.2502A>C
NM_000527.5:c.2525A>C MANE Select NP_000518.1:p.Gln842Pro
NM_001195798.2:c.2525A>C NP_001182727.1:p.Gln842Pro
NM_001195799.2:c.2402A>C NP_001182728.1:p.Gln801Pro
NM_001195800.2:c.2021A>C NP_001182729.1:p.Gln674Pro
NM_001195803.2:c.1991A>C NP_001182732.1:p.Gln664Pro