Canonical Allele Identifier: CA2322767358

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11105313A= , CM000681.2:g.11105313A=	GRCh38
NC_000019.9:g.11215989A= , CM000681.1:g.11215989A=	GRCh37
NC_000019.8:g.11076989A=	NCBI36
NG_009060.1:g.20933A= , LRG_274:g.20933A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.665A=	ENSP00000252444.6:p.Asp222=
ENST00000559340.2:c.407A=	ENSP00000453696.2:p.Asp136=
ENST00000560467.2:c.407A=	ENSP00000453513.2:p.Asp136=
ENST00000558518.6:c.407A= MANE Select	ENSP00000454071.1:p.Asp136=
ENST00000252444.9:c.661A=
ENST00000455727.6:c.314-2079A=	ENSP00000397829.2:n.314-2079A=
ENST00000535915.5:c.284A=	ENSP00000440520.1:p.Asp95=
ENST00000545707.5:c.314-1252A=	ENSP00000437639.1:n.314-1252A=
ENST00000557933.5:c.407A=	ENSP00000453557.1:p.Asp136=
ENST00000558013.5:c.407A=	ENSP00000453346.1:p.Asp136=
ENST00000558518.5:c.407A=	ENSP00000454071.1:p.Asp136=
ENST00000560467.1:c.7A=
NM_000527.4:c.407A= , LRG_274t1:c.407A=	NP_000518.1:p.Asp136=
NM_001195798.1:c.407A=	NP_001182727.1:p.Asp136=
NM_001195799.1:c.284A=	NP_001182728.1:p.Asp95=
NM_001195800.1:c.314-2079A=	NP_001182729.1:n.314-2079A=
NM_001195803.1:c.314-1252A=	NP_001182732.1:n.314-1252A=
XM_011528010.1:c.407A=	XP_011526312.1:p.Asp136=
XM_011528011.1:c.314-1252A=	XP_011526313.1:n.314-1252A=
XR_244074.2:n.557A=
XM_011528010.2:c.407A=	XP_011526312.1:p.Asp136=
XR_001753685.2:n.524A=
XR_001753686.2:n.524A=
NM_000527.5:c.407A= MANE Select	NP_000518.1:p.Asp136=
NM_001195798.2:c.407A=	NP_001182727.1:p.Asp136=
NM_001195799.2:c.284A=	NP_001182728.1:p.Asp95=
NM_001195800.2:c.314-2079A=	NP_001182729.1:n.314-2079A=
NM_001195803.2:c.314-1252A=	NP_001182732.1:n.314-1252A=