Canonical Allele Identifier: CA404080801

Gene: LDLR

Linked Data

• ClinVar Variation Id: 2858988
• ClinVar RCV Id: RCV003742286
• MyVariant Identifiers: chr19:g.11218117C>A (hg19) ; chr19:g.11107441C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107441C>A , CM000681.2:g.11107441C>A	GRCh38
NC_000019.9:g.11218117C>A , CM000681.1:g.11218117C>A	GRCh37
NC_000019.8:g.11079117C>A	NCBI36
NG_009060.1:g.23061C>A , LRG_274:g.23061C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1125C>A	ENSP00000252444.6:p.Cys375Ter
ENST00000559340.2:c.867C>A	ENSP00000453696.2:p.Cys289Ter
ENST00000560467.2:c.867C>A	ENSP00000453513.2:p.Cys289Ter
ENST00000558518.6:c.867C>A MANE Select	ENSP00000454071.1:p.Cys289Ter
ENST00000252444.9:c.1121C>A
ENST00000455727.6:c.363C>A	ENSP00000397829.2:p.Cys121Ter
ENST00000535915.5:c.744C>A	ENSP00000440520.1:p.Cys248Ter
ENST00000545707.5:c.486C>A	ENSP00000437639.1:p.Cys162Ter
ENST00000557933.5:c.867C>A	ENSP00000453557.1:p.Cys289Ter
ENST00000558013.5:c.867C>A	ENSP00000453346.1:p.Cys289Ter
ENST00000558518.5:c.867C>A	ENSP00000454071.1:p.Cys289Ter
ENST00000558528.1:n.382C>A
ENST00000560467.1:c.467C>A
NM_000527.4:c.867C>A , LRG_274t1:c.867C>A	NP_000518.1:p.Cys289Ter
NM_001195798.1:c.867C>A	NP_001182727.1:p.Cys289Ter
NM_001195799.1:c.744C>A	NP_001182728.1:p.Cys248Ter
NM_001195800.1:c.363C>A	NP_001182729.1:p.Cys121Ter
NM_001195803.1:c.486C>A	NP_001182732.1:p.Cys162Ter
XM_011528010.1:c.867C>A	XP_011526312.1:p.Cys289Ter
XM_011528011.1:c.486C>A	XP_011526313.1:p.Cys162Ter
XR_244074.2:n.1017C>A
XM_011528010.2:c.867C>A	XP_011526312.1:p.Cys289Ter
XR_001753685.2:n.984C>A
XR_001753686.2:n.984C>A
NM_000527.5:c.867C>A MANE Select	NP_000518.1:p.Cys289Ter
NM_001195798.2:c.867C>A	NP_001182727.1:p.Cys289Ter
NM_001195799.2:c.744C>A	NP_001182728.1:p.Cys248Ter
NM_001195800.2:c.363C>A	NP_001182729.1:p.Cys121Ter
NM_001195803.2:c.486C>A	NP_001182732.1:p.Cys162Ter