Canonical Allele Identifier: CA10585555

Gene: LDLR

Linked Data

• ClinVar Variation Id: 251964
• ClinVar RCV Id: RCV000237630
• dbSNP Id: rs879254980
• MyVariant Identifiers: chr19:g.11226855G>T (hg19) ; chr19:g.11116179G>T (hg38)
• PubMed: PMID:21310417 ; PMID:22698793

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11116179G>T , CM000681.2:g.11116179G>T	GRCh38
NC_000019.9:g.11226855G>T , CM000681.1:g.11226855G>T	GRCh37
NC_000019.8:g.11087855G>T	NCBI36
NG_009060.1:g.31799G>T , LRG_274:g.31799G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1930G>T	ENSP00000252444.6:p.Glu644Ter
ENST00000559340.2:c.1672G>T	ENSP00000453696.2:p.Glu558Ter
ENST00000560467.2:c.1552G>T	ENSP00000453513.2:p.Glu518Ter
ENST00000558518.6:c.1672G>T MANE Select	ENSP00000454071.1:p.Glu558Ter
ENST00000252444.9:c.1926G>T
ENST00000455727.6:c.1168G>T	ENSP00000397829.2:p.Glu390Ter
ENST00000535915.5:c.1549G>T	ENSP00000440520.1:p.Glu517Ter
ENST00000545707.5:c.1291G>T	ENSP00000437639.1:p.Glu431Ter
ENST00000557933.5:c.1672G>T	ENSP00000453557.1:p.Glu558Ter
ENST00000558013.5:c.1672G>T	ENSP00000453346.1:p.Glu558Ter
ENST00000558518.5:c.1672G>T	ENSP00000454071.1:p.Glu558Ter
ENST00000559340.1:c.393G>T
NM_000527.4:c.1672G>T , LRG_274t1:c.1672G>T	NP_000518.1:p.Glu558Ter
NM_001195798.1:c.1672G>T	NP_001182727.1:p.Glu558Ter
NM_001195799.1:c.1549G>T	NP_001182728.1:p.Glu517Ter
NM_001195800.1:c.1168G>T	NP_001182729.1:p.Glu390Ter
NM_001195803.1:c.1291G>T	NP_001182732.1:p.Glu431Ter
XM_011528010.1:c.1672G>T	XP_011526312.1:p.Glu558Ter
XM_011528011.1:c.1291G>T	XP_011526313.1:p.Glu431Ter
XR_244074.2:n.1822G>T
XM_011528010.2:c.1672G>T	XP_011526312.1:p.Glu558Ter
XR_001753685.2:n.1789G>T
XR_001753686.2:n.1789G>T
NM_000527.5:c.1672G>T MANE Select	NP_000518.1:p.Glu558Ter
NM_001195798.2:c.1672G>T	NP_001182727.1:p.Glu558Ter
NM_001195799.2:c.1549G>T	NP_001182728.1:p.Glu517Ter
NM_001195800.2:c.1168G>T	NP_001182729.1:p.Glu390Ter
NM_001195803.2:c.1291G>T	NP_001182732.1:p.Glu431Ter