Canonical Allele Identifier: CA2322771790

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113416A= , CM000681.2:g.11113416A=	GRCh38
NC_000019.9:g.11224092A= , CM000681.1:g.11224092A=	GRCh37
NC_000019.8:g.11085092A=	NCBI36
NG_009060.1:g.29036A= , LRG_274:g.29036A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1583A=	ENSP00000252444.6:p.Tyr528=
ENST00000559340.2:c.1325A=	ENSP00000453696.2:p.Tyr442=
ENST00000560467.2:c.1205A=	ENSP00000453513.2:p.Tyr402=
ENST00000558518.6:c.1325A= MANE Select	ENSP00000454071.1:p.Tyr442=
ENST00000252444.9:c.1579A=
ENST00000455727.6:c.821A=	ENSP00000397829.2:p.Tyr274=
ENST00000535915.5:c.1202A=	ENSP00000440520.1:p.Tyr401=
ENST00000545707.5:c.944A=	ENSP00000437639.1:p.Tyr315=
ENST00000557933.5:c.1325A=	ENSP00000453557.1:p.Tyr442=
ENST00000558013.5:c.1325A=	ENSP00000453346.1:p.Tyr442=
ENST00000558518.5:c.1325A=	ENSP00000454071.1:p.Tyr442=
ENST00000559340.1:c.46A=
ENST00000560173.1:n.324A=
ENST00000560467.1:c.805A=
NM_000527.4:c.1325A= , LRG_274t1:c.1325A=	NP_000518.1:p.Tyr442=
NM_001195798.1:c.1325A=	NP_001182727.1:p.Tyr442=
NM_001195799.1:c.1202A=	NP_001182728.1:p.Tyr401=
NM_001195800.1:c.821A=	NP_001182729.1:p.Tyr274=
NM_001195803.1:c.944A=	NP_001182732.1:p.Tyr315=
XM_011528010.1:c.1325A=	XP_011526312.1:p.Tyr442=
XM_011528011.1:c.944A=	XP_011526313.1:p.Tyr315=
XR_244074.2:n.1475A=
XM_011528010.2:c.1325A=	XP_011526312.1:p.Tyr442=
XR_001753685.2:n.1442A=
XR_001753686.2:n.1442A=
NM_000527.5:c.1325A= MANE Select	NP_000518.1:p.Tyr442=
NM_001195798.2:c.1325A=	NP_001182727.1:p.Tyr442=
NM_001195799.2:c.1202A=	NP_001182728.1:p.Tyr401=
NM_001195800.2:c.821A=	NP_001182729.1:p.Tyr274=
NM_001195803.2:c.944A=	NP_001182732.1:p.Tyr315=