Canonical Allele Identifier: CA404093003

Gene: LDLR

Linked Data

• gnomAD v4: 19-11120178-A-C
• MyVariant Identifiers: chr19:g.11230854A>C (hg19) ; chr19:g.11120178A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120178A>C , CM000681.2:g.11120178A>C	GRCh38
NC_000019.9:g.11230854A>C , CM000681.1:g.11230854A>C	GRCh37
NC_000019.8:g.11091854A>C	NCBI36
NG_009060.1:g.35798A>C , LRG_274:g.35798A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2190A>C	ENSP00000252444.6:p.Glu730Asp
ENST00000559340.2:c.*1A>C	ENSP00000453696.2:n.*1A>C
ENST00000560467.2:c.1812A>C	ENSP00000453513.2:p.Glu604Asp
ENST00000558518.6:c.1932A>C MANE Select	ENSP00000454071.1:p.Glu644Asp
ENST00000252444.9:c.2186A>C
ENST00000455727.6:c.1428A>C	ENSP00000397829.2:p.Glu476Asp
ENST00000535915.5:c.1809A>C	ENSP00000440520.1:p.Glu603Asp
ENST00000545707.5:c.1551A>C	ENSP00000437639.1:p.Glu517Asp
ENST00000557933.5:c.1932A>C	ENSP00000453557.1:p.Glu644Asp
ENST00000558013.5:c.1932A>C	ENSP00000453346.1:p.Glu644Asp
ENST00000558518.5:c.1932A>C	ENSP00000454071.1:p.Glu644Asp
ENST00000559340.1:c.513A>C
NM_000527.4:c.1932A>C , LRG_274t1:c.1932A>C	NP_000518.1:p.Glu644Asp
NM_001195798.1:c.1932A>C	NP_001182727.1:p.Glu644Asp
NM_001195799.1:c.1809A>C	NP_001182728.1:p.Glu603Asp
NM_001195800.1:c.1428A>C	NP_001182729.1:p.Glu476Asp
NM_001195803.1:c.1551A>C	NP_001182732.1:p.Glu517Asp
XM_011528010.1:c.1932A>C	XP_011526312.1:p.Glu644Asp
XM_011528011.1:c.1551A>C	XP_011526313.1:p.Glu517Asp
XR_244074.2:n.1942A>C
XM_011528010.2:c.1932A>C	XP_011526312.1:p.Glu644Asp
XR_001753685.2:n.2049A>C
XR_001753686.2:n.1909A>C
NM_000527.5:c.1932A>C MANE Select	NP_000518.1:p.Glu644Asp
NM_001195798.2:c.1932A>C	NP_001182727.1:p.Glu644Asp
NM_001195799.2:c.1809A>C	NP_001182728.1:p.Glu603Asp
NM_001195800.2:c.1428A>C	NP_001182729.1:p.Glu476Asp
NM_001195803.2:c.1551A>C	NP_001182732.1:p.Glu517Asp