Canonical Allele Identifier: CA2322771787

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11113413T= , CM000681.2:g.11113413T=	GRCh38
NC_000019.9:g.11224089T= , CM000681.1:g.11224089T=	GRCh37
NC_000019.8:g.11085089T=	NCBI36
NG_009060.1:g.29033T= , LRG_274:g.29033T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.1580T=	ENSP00000252444.6:p.Ile527=
ENST00000559340.2:c.1322T=	ENSP00000453696.2:p.Ile441=
ENST00000560467.2:c.1202T=	ENSP00000453513.2:p.Ile401=
ENST00000558518.6:c.1322T= MANE Select	ENSP00000454071.1:p.Ile441=
ENST00000252444.9:c.1576T=
ENST00000455727.6:c.818T=	ENSP00000397829.2:p.Ile273=
ENST00000535915.5:c.1199T=	ENSP00000440520.1:p.Ile400=
ENST00000545707.5:c.941T=	ENSP00000437639.1:p.Ile314=
ENST00000557933.5:c.1322T=	ENSP00000453557.1:p.Ile441=
ENST00000558013.5:c.1322T=	ENSP00000453346.1:p.Ile441=
ENST00000558518.5:c.1322T=	ENSP00000454071.1:p.Ile441=
ENST00000559340.1:c.43T=
ENST00000560173.1:n.321T=
ENST00000560467.1:c.802T=
NM_000527.4:c.1322T= , LRG_274t1:c.1322T=	NP_000518.1:p.Ile441=
NM_001195798.1:c.1322T=	NP_001182727.1:p.Ile441=
NM_001195799.1:c.1199T=	NP_001182728.1:p.Ile400=
NM_001195800.1:c.818T=	NP_001182729.1:p.Ile273=
NM_001195803.1:c.941T=	NP_001182732.1:p.Ile314=
XM_011528010.1:c.1322T=	XP_011526312.1:p.Ile441=
XM_011528011.1:c.941T=	XP_011526313.1:p.Ile314=
XR_244074.2:n.1472T=
XM_011528010.2:c.1322T=	XP_011526312.1:p.Ile441=
XR_001753685.2:n.1439T=
XR_001753686.2:n.1439T=
NM_000527.5:c.1322T= MANE Select	NP_000518.1:p.Ile441=
NM_001195798.2:c.1322T=	NP_001182727.1:p.Ile441=
NM_001195799.2:c.1199T=	NP_001182728.1:p.Ile400=
NM_001195800.2:c.818T=	NP_001182729.1:p.Ile273=
NM_001195803.2:c.941T=	NP_001182732.1:p.Ile314=