Canonical Allele Identifier: CA404099180
Gene: LDLR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11129597A>T , CM000681.2:g.11129597A>T GRCh38
NC_000019.9:g.11240273A>T , CM000681.1:g.11240273A>T GRCh37
NC_000019.8:g.11101273A>T NCBI36
NG_009060.1:g.45217A>T , LRG_274:g.45217A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252444.10:c.2732A>T ENSP00000252444.6:p.Asn911Ile
ENST00000559340.2:c.*543A>T ENSP00000453696.2:n.*543A>T
ENST00000560467.2:c.2354A>T ENSP00000453513.2:p.Asn785Ile
ENST00000558518.6:c.2474A>T MANE Select ENSP00000454071.1:p.Asn825Ile
ENST00000252444.9:c.2728A>T
ENST00000455727.6:c.1970A>T ENSP00000397829.2:p.Asn657Ile
ENST00000535915.5:c.2351A>T ENSP00000440520.1:p.Asn784Ile
ENST00000545707.5:c.1940A>T ENSP00000437639.1:p.Asn647Ile
ENST00000557933.5:c.2536A>T ENSP00000453557.1:p.Thr846Ser
ENST00000558013.5:c.2474A>T ENSP00000453346.1:p.Asn825Ile
ENST00000558518.5:c.2474A>T ENSP00000454071.1:p.Asn825Ile
ENST00000560628.1:n.108+1943A>T
NM_000527.4:c.2474A>T , LRG_274t1:c.2474A>T NP_000518.1:p.Asn825Ile
NM_001195798.1:c.2474A>T NP_001182727.1:p.Asn825Ile
NM_001195799.1:c.2351A>T NP_001182728.1:p.Asn784Ile
NM_001195800.1:c.1970A>T NP_001182729.1:p.Asn657Ile
NM_001195803.1:c.1940A>T NP_001182732.1:p.Asn647Ile
XM_011528010.1:c.2396A>T XP_011526312.1:p.Asn799Ile
XM_011528011.1:c.2093A>T XP_011526313.1:p.Asn698Ile
XM_011528010.2:c.2396A>T XP_011526312.1:p.Asn799Ile
XR_001753685.2:n.2808A>T
XR_001753686.2:n.2451A>T
NM_000527.5:c.2474A>T MANE Select NP_000518.1:p.Asn825Ile
NM_001195798.2:c.2474A>T NP_001182727.1:p.Asn825Ile
NM_001195799.2:c.2351A>T NP_001182728.1:p.Asn784Ile
NM_001195800.2:c.1970A>T NP_001182729.1:p.Asn657Ile
NM_001195803.2:c.1940A>T NP_001182732.1:p.Asn647Ile