Canonical Allele Identifier: CA2322775626

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120471G= , CM000681.2:g.11120471G=	GRCh38
NC_000019.9:g.11231147G= , CM000681.1:g.11231147G=	GRCh37
NC_000019.8:g.11092147G=	NCBI36
NG_009060.1:g.36091G= , LRG_274:g.36091G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2347G=	ENSP00000252444.6:p.Ala783=
ENST00000559340.2:c.*158G=	ENSP00000453696.2:n.*158G=
ENST00000560467.2:c.1969G=	ENSP00000453513.2:p.Ala657=
ENST00000558518.6:c.2089G= MANE Select	ENSP00000454071.1:p.Ala697=
ENST00000252444.9:c.2343G=
ENST00000455727.6:c.1585G=	ENSP00000397829.2:p.Ala529=
ENST00000535915.5:c.1966G=	ENSP00000440520.1:p.Ala656=
ENST00000545707.5:c.1606+238G=	ENSP00000437639.1:n.1606+238G=
ENST00000557933.5:c.2089G=	ENSP00000453557.1:p.Ala697=
ENST00000558013.5:c.2089G=	ENSP00000453346.1:p.Ala697=
ENST00000558518.5:c.2089G=	ENSP00000454071.1:p.Ala697=
NM_000527.4:c.2089G= , LRG_274t1:c.2089G=	NP_000518.1:p.Ala697=
NM_001195798.1:c.2089G=	NP_001182727.1:p.Ala697=
NM_001195799.1:c.1966G=	NP_001182728.1:p.Ala656=
NM_001195800.1:c.1585G=	NP_001182729.1:p.Ala529=
NM_001195803.1:c.1606+238G=	NP_001182732.1:n.1606+238G=
XM_011528010.1:c.2089G=	XP_011526312.1:p.Ala697=
XM_011528011.1:c.1708G=	XP_011526313.1:p.Ala570=
XR_244074.2:n.2099G=
XM_011528010.2:c.2089G=	XP_011526312.1:p.Ala697=
XR_001753685.2:n.2206G=
XR_001753686.2:n.2066G=
NM_000527.5:c.2089G= MANE Select	NP_000518.1:p.Ala697=
NM_001195798.2:c.2089G=	NP_001182727.1:p.Ala697=
NM_001195799.2:c.1966G=	NP_001182728.1:p.Ala656=
NM_001195800.2:c.1585G=	NP_001182729.1:p.Ala529=
NM_001195803.2:c.1606+238G=	NP_001182732.1:n.1606+238G=