Canonical Allele Identifier: CA2322771794

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113420G= , CM000681.2:g.11113420G=	GRCh38
NC_000019.9:g.11224096G= , CM000681.1:g.11224096G=	GRCh37
NC_000019.8:g.11085096G=	NCBI36
NG_009060.1:g.29040G= , LRG_274:g.29040G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1587G=	ENSP00000252444.6:p.Trp529=
ENST00000559340.2:c.1329G=	ENSP00000453696.2:p.Trp443=
ENST00000560467.2:c.1209G=	ENSP00000453513.2:p.Trp403=
ENST00000558518.6:c.1329G= MANE Select	ENSP00000454071.1:p.Trp443=
ENST00000252444.9:c.1583G=
ENST00000455727.6:c.825G=	ENSP00000397829.2:p.Trp275=
ENST00000535915.5:c.1206G=	ENSP00000440520.1:p.Trp402=
ENST00000545707.5:c.948G=	ENSP00000437639.1:p.Trp316=
ENST00000557933.5:c.1329G=	ENSP00000453557.1:p.Trp443=
ENST00000558013.5:c.1329G=	ENSP00000453346.1:p.Trp443=
ENST00000558518.5:c.1329G=	ENSP00000454071.1:p.Trp443=
ENST00000559340.1:c.50G=
ENST00000560173.1:n.328G=
ENST00000560467.1:c.809G=
NM_000527.4:c.1329G= , LRG_274t1:c.1329G=	NP_000518.1:p.Trp443=
NM_001195798.1:c.1329G=	NP_001182727.1:p.Trp443=
NM_001195799.1:c.1206G=	NP_001182728.1:p.Trp402=
NM_001195800.1:c.825G=	NP_001182729.1:p.Trp275=
NM_001195803.1:c.948G=	NP_001182732.1:p.Trp316=
XM_011528010.1:c.1329G=	XP_011526312.1:p.Trp443=
XM_011528011.1:c.948G=	XP_011526313.1:p.Trp316=
XR_244074.2:n.1479G=
XM_011528010.2:c.1329G=	XP_011526312.1:p.Trp443=
XR_001753685.2:n.1446G=
XR_001753686.2:n.1446G=
NM_000527.5:c.1329G= MANE Select	NP_000518.1:p.Trp443=
NM_001195798.2:c.1329G=	NP_001182727.1:p.Trp443=
NM_001195799.2:c.1206G=	NP_001182728.1:p.Trp402=
NM_001195800.2:c.825G=	NP_001182729.1:p.Trp275=
NM_001195803.2:c.948G=	NP_001182732.1:p.Trp316=