Canonical Allele Identifier: CA404088538

Gene: LDLR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11116101T>A , CM000681.2:g.11116101T>A	GRCh38
NC_000019.9:g.11226777T>A , CM000681.1:g.11226777T>A	GRCh37
NC_000019.8:g.11087777T>A	NCBI36
NG_009060.1:g.31721T>A , LRG_274:g.31721T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1852T>A	ENSP00000252444.6:p.Tyr618Asn
ENST00000559340.2:c.1594T>A	ENSP00000453696.2:p.Tyr532Asn
ENST00000560467.2:c.1474T>A	ENSP00000453513.2:p.Tyr492Asn
ENST00000558518.6:c.1594T>A MANE Select	ENSP00000454071.1:p.Tyr532Asn
ENST00000252444.9:c.1848T>A
ENST00000455727.6:c.1090T>A	ENSP00000397829.2:p.Tyr364Asn
ENST00000535915.5:c.1471T>A	ENSP00000440520.1:p.Tyr491Asn
ENST00000545707.5:c.1213T>A	ENSP00000437639.1:p.Tyr405Asn
ENST00000557933.5:c.1594T>A	ENSP00000453557.1:p.Tyr532Asn
ENST00000558013.5:c.1594T>A	ENSP00000453346.1:p.Tyr532Asn
ENST00000558518.5:c.1594T>A	ENSP00000454071.1:p.Tyr532Asn
ENST00000559340.1:c.315T>A
NM_000527.4:c.1594T>A , LRG_274t1:c.1594T>A	NP_000518.1:p.Tyr532Asn
NM_001195798.1:c.1594T>A	NP_001182727.1:p.Tyr532Asn
NM_001195799.1:c.1471T>A	NP_001182728.1:p.Tyr491Asn
NM_001195800.1:c.1090T>A	NP_001182729.1:p.Tyr364Asn
NM_001195803.1:c.1213T>A	NP_001182732.1:p.Tyr405Asn
XM_011528010.1:c.1594T>A	XP_011526312.1:p.Tyr532Asn
XM_011528011.1:c.1213T>A	XP_011526313.1:p.Tyr405Asn
XR_244074.2:n.1744T>A
XM_011528010.2:c.1594T>A	XP_011526312.1:p.Tyr532Asn
XR_001753685.2:n.1711T>A
XR_001753686.2:n.1711T>A
NM_000527.5:c.1594T>A MANE Select	NP_000518.1:p.Tyr532Asn
NM_001195798.2:c.1594T>A	NP_001182727.1:p.Tyr532Asn
NM_001195799.2:c.1471T>A	NP_001182728.1:p.Tyr491Asn
NM_001195800.2:c.1090T>A	NP_001182729.1:p.Tyr364Asn
NM_001195803.2:c.1213T>A	NP_001182732.1:p.Tyr405Asn