Canonical Allele Identifier: CA404094788
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11123188G>A , CM000681.2:g.11123188G>A GRCh38
NC_000019.9:g.11233864G>A , CM000681.1:g.11233864G>A GRCh37
NC_000019.8:g.11094864G>A NCBI36
NG_009060.1:g.38808G>A , LRG_274:g.38808G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2413G>A ENSP00000252444.6:p.Val805Met
ENST00000559340.2:c.*224G>A ENSP00000453696.2:n.*224G>A
ENST00000560467.2:c.2035G>A ENSP00000453513.2:p.Val679Met
ENST00000558518.6:c.2155G>A MANE Select ENSP00000454071.1:p.Val719Met
ENST00000252444.9:c.2409G>A
ENST00000455727.6:c.1651G>A ENSP00000397829.2:p.Val551Met
ENST00000535915.5:c.2032G>A ENSP00000440520.1:p.Val678Met
ENST00000545707.5:c.1621G>A ENSP00000437639.1:p.Val541Met
ENST00000557933.5:c.2155G>A ENSP00000453557.1:p.Val719Met
ENST00000558013.5:c.2155G>A ENSP00000453346.1:p.Val719Met
ENST00000558518.5:c.2155G>A ENSP00000454071.1:p.Val719Met
NM_000527.4:c.2155G>A , LRG_274t1:c.2155G>A NP_000518.1:p.Val719Met
NM_001195798.1:c.2155G>A NP_001182727.1:p.Val719Met
NM_001195799.1:c.2032G>A NP_001182728.1:p.Val678Met
NM_001195800.1:c.1651G>A NP_001182729.1:p.Val551Met
NM_001195803.1:c.1621G>A NP_001182732.1:p.Val541Met
XM_011528010.1:c.2155G>A XP_011526312.1:p.Val719Met
XM_011528011.1:c.1774G>A XP_011526313.1:p.Val592Met
XR_244074.2:n.2165G>A
XM_011528010.2:c.2155G>A XP_011526312.1:p.Val719Met
XR_001753685.2:n.2489G>A
XR_001753686.2:n.2132G>A
NM_000527.5:c.2155G>A MANE Select NP_000518.1:p.Val719Met
NM_001195798.2:c.2155G>A NP_001182727.1:p.Val719Met
NM_001195799.2:c.2032G>A NP_001182728.1:p.Val678Met
NM_001195800.2:c.1651G>A NP_001182729.1:p.Val551Met
NM_001195803.2:c.1621G>A NP_001182732.1:p.Val541Met