Canonical Allele Identifier: CA2322775369

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120129T= , CM000681.2:g.11120129T=	GRCh38
NC_000019.9:g.11230805T= , CM000681.1:g.11230805T=	GRCh37
NC_000019.8:g.11091805T=	NCBI36
NG_009060.1:g.35749T= , LRG_274:g.35749T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2141T=	ENSP00000252444.6:p.Ile714=
ENST00000559340.2:c.1743T=	ENSP00000453696.2:p.His581=
ENST00000560467.2:c.1763T=	ENSP00000453513.2:p.Ile588=
ENST00000558518.6:c.1883T= MANE Select	ENSP00000454071.1:p.Ile628=
ENST00000252444.9:c.2137T=
ENST00000455727.6:c.1379T=	ENSP00000397829.2:p.Ile460=
ENST00000535915.5:c.1760T=	ENSP00000440520.1:p.Ile587=
ENST00000545707.5:c.1502T=	ENSP00000437639.1:p.Ile501=
ENST00000557933.5:c.1883T=	ENSP00000453557.1:p.Ile628=
ENST00000558013.5:c.1883T=	ENSP00000453346.1:p.Ile628=
ENST00000558518.5:c.1883T=	ENSP00000454071.1:p.Ile628=
ENST00000559340.1:c.464T=
NM_000527.4:c.1883T= , LRG_274t1:c.1883T=	NP_000518.1:p.Ile628=
NM_001195798.1:c.1883T=	NP_001182727.1:p.Ile628=
NM_001195799.1:c.1760T=	NP_001182728.1:p.Ile587=
NM_001195800.1:c.1379T=	NP_001182729.1:p.Ile460=
NM_001195803.1:c.1502T=	NP_001182732.1:p.Ile501=
XM_011528010.1:c.1883T=	XP_011526312.1:p.Ile628=
XM_011528011.1:c.1502T=	XP_011526313.1:p.Ile501=
XR_244074.2:n.1893T=
XM_011528010.2:c.1883T=	XP_011526312.1:p.Ile628=
XR_001753685.2:n.2000T=
XR_001753686.2:n.1860T=
NM_000527.5:c.1883T= MANE Select	NP_000518.1:p.Ile628=
NM_001195798.2:c.1883T=	NP_001182727.1:p.Ile628=
NM_001195799.2:c.1760T=	NP_001182728.1:p.Ile587=
NM_001195800.2:c.1379T=	NP_001182729.1:p.Ile460=
NM_001195803.2:c.1502T=	NP_001182732.1:p.Ile501=