Canonical Allele Identifier: CA404080927

Gene: LDLR

Linked Data

• ClinVar Variation Id: 1764881
• ClinVar RCV Id: RCV002373828
• MyVariant Identifiers: chr19:g.11218134T>G (hg19) ; chr19:g.11107458T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107458T>G , CM000681.2:g.11107458T>G	GRCh38
NC_000019.9:g.11218134T>G , CM000681.1:g.11218134T>G	GRCh37
NC_000019.8:g.11079134T>G	NCBI36
NG_009060.1:g.23078T>G , LRG_274:g.23078T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1142T>G	ENSP00000252444.6:p.Val381Gly
ENST00000559340.2:c.884T>G	ENSP00000453696.2:p.Val295Gly
ENST00000560467.2:c.884T>G	ENSP00000453513.2:p.Val295Gly
ENST00000558518.6:c.884T>G MANE Select	ENSP00000454071.1:p.Val295Gly
ENST00000252444.9:c.1138T>G
ENST00000455727.6:c.380T>G	ENSP00000397829.2:p.Val127Gly
ENST00000535915.5:c.761T>G	ENSP00000440520.1:p.Val254Gly
ENST00000545707.5:c.503T>G	ENSP00000437639.1:p.Val168Gly
ENST00000557933.5:c.884T>G	ENSP00000453557.1:p.Val295Gly
ENST00000558013.5:c.884T>G	ENSP00000453346.1:p.Val295Gly
ENST00000558518.5:c.884T>G	ENSP00000454071.1:p.Val295Gly
ENST00000558528.1:n.399T>G
ENST00000560467.1:c.484T>G
NM_000527.4:c.884T>G , LRG_274t1:c.884T>G	NP_000518.1:p.Val295Gly
NM_001195798.1:c.884T>G	NP_001182727.1:p.Val295Gly
NM_001195799.1:c.761T>G	NP_001182728.1:p.Val254Gly
NM_001195800.1:c.380T>G	NP_001182729.1:p.Val127Gly
NM_001195803.1:c.503T>G	NP_001182732.1:p.Val168Gly
XM_011528010.1:c.884T>G	XP_011526312.1:p.Val295Gly
XM_011528011.1:c.503T>G	XP_011526313.1:p.Val168Gly
XR_244074.2:n.1034T>G
XM_011528010.2:c.884T>G	XP_011526312.1:p.Val295Gly
XR_001753685.2:n.1001T>G
XR_001753686.2:n.1001T>G
NM_000527.5:c.884T>G MANE Select	NP_000518.1:p.Val295Gly
NM_001195798.2:c.884T>G	NP_001182727.1:p.Val295Gly
NM_001195799.2:c.761T>G	NP_001182728.1:p.Val254Gly
NM_001195800.2:c.380T>G	NP_001182729.1:p.Val127Gly
NM_001195803.2:c.503T>G	NP_001182732.1:p.Val168Gly