Canonical Allele Identifier: CA505485650

Gene: LDLR

Linked Data

• MyVariant Identifiers: chr19:g.11222311T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11111635T>C , CM000681.2:g.11111635T>C	GRCh38
NC_000019.9:g.11222311T>C , CM000681.1:g.11222311T>C	GRCh37
NC_000019.8:g.11083311T>C	NCBI36
NG_009060.1:g.27255T>C , LRG_274:g.27255T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1440T>C	ENSP00000252444.6:p.Ala480=
ENST00000559340.2:c.1182T>C	ENSP00000453696.2:p.Ala394=
ENST00000560467.2:c.1062T>C	ENSP00000453513.2:p.Ala354=
ENST00000558518.6:c.1182T>C MANE Select	ENSP00000454071.1:p.Ala394=
ENST00000252444.9:c.1436T>C
ENST00000455727.6:c.678T>C	ENSP00000397829.2:p.Ala226=
ENST00000535915.5:c.1059T>C	ENSP00000440520.1:p.Ala353=
ENST00000545707.5:c.801T>C	ENSP00000437639.1:p.Ala267=
ENST00000557933.5:c.1182T>C	ENSP00000453557.1:p.Ala394=
ENST00000558013.5:c.1182T>C	ENSP00000453346.1:p.Ala394=
ENST00000558518.5:c.1182T>C	ENSP00000454071.1:p.Ala394=
ENST00000560173.1:n.181T>C
ENST00000560467.1:c.662T>C
NM_000527.4:c.1182T>C , LRG_274t1:c.1182T>C	NP_000518.1:p.Ala394=
NM_001195798.1:c.1182T>C	NP_001182727.1:p.Ala394=
NM_001195799.1:c.1059T>C	NP_001182728.1:p.Ala353=
NM_001195800.1:c.678T>C	NP_001182729.1:p.Ala226=
NM_001195803.1:c.801T>C	NP_001182732.1:p.Ala267=
XM_011528010.1:c.1182T>C	XP_011526312.1:p.Ala394=
XM_011528011.1:c.801T>C	XP_011526313.1:p.Ala267=
XR_244074.2:n.1332T>C
XM_011528010.2:c.1182T>C	XP_011526312.1:p.Ala394=
XR_001753685.2:n.1299T>C
XR_001753686.2:n.1299T>C
NM_000527.5:c.1182T>C MANE Select	NP_000518.1:p.Ala394=
NM_001195798.2:c.1182T>C	NP_001182727.1:p.Ala394=
NM_001195799.2:c.1059T>C	NP_001182728.1:p.Ala353=
NM_001195800.2:c.678T>C	NP_001182729.1:p.Ala226=
NM_001195803.2:c.801T>C	NP_001182732.1:p.Ala267=