Canonical Allele Identifier: CA2322768593

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11107433G= , CM000681.2:g.11107433G=	GRCh38
NC_000019.9:g.11218109G= , CM000681.1:g.11218109G=	GRCh37
NC_000019.8:g.11079109G=	NCBI36
NG_009060.1:g.23053G= , LRG_274:g.23053G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.1117G=	ENSP00000252444.6:p.Gly373=
ENST00000559340.2:c.859G=	ENSP00000453696.2:p.Gly287=
ENST00000560467.2:c.859G=	ENSP00000453513.2:p.Gly287=
ENST00000558518.6:c.859G= MANE Select	ENSP00000454071.1:p.Gly287=
ENST00000252444.9:c.1113G=
ENST00000455727.6:c.355G=	ENSP00000397829.2:p.Gly119=
ENST00000535915.5:c.736G=	ENSP00000440520.1:p.Gly246=
ENST00000545707.5:c.478G=	ENSP00000437639.1:p.Gly160=
ENST00000557933.5:c.859G=	ENSP00000453557.1:p.Gly287=
ENST00000558013.5:c.859G=	ENSP00000453346.1:p.Gly287=
ENST00000558518.5:c.859G=	ENSP00000454071.1:p.Gly287=
ENST00000558528.1:n.374G=
ENST00000560467.1:c.459G=
NM_000527.4:c.859G= , LRG_274t1:c.859G=	NP_000518.1:p.Gly287=
NM_001195798.1:c.859G=	NP_001182727.1:p.Gly287=
NM_001195799.1:c.736G=	NP_001182728.1:p.Gly246=
NM_001195800.1:c.355G=	NP_001182729.1:p.Gly119=
NM_001195803.1:c.478G=	NP_001182732.1:p.Gly160=
XM_011528010.1:c.859G=	XP_011526312.1:p.Gly287=
XM_011528011.1:c.478G=	XP_011526313.1:p.Gly160=
XR_244074.2:n.1009G=
XM_011528010.2:c.859G=	XP_011526312.1:p.Gly287=
XR_001753685.2:n.976G=
XR_001753686.2:n.976G=
NM_000527.5:c.859G= MANE Select	NP_000518.1:p.Gly287=
NM_001195798.2:c.859G=	NP_001182727.1:p.Gly287=
NM_001195799.2:c.736G=	NP_001182728.1:p.Gly246=
NM_001195800.2:c.355G=	NP_001182729.1:p.Gly119=
NM_001195803.2:c.478G=	NP_001182732.1:p.Gly160=