Canonical Allele Identifier: CA2322777168

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11123186C= , CM000681.2:g.11123186C=	GRCh38
NC_000019.9:g.11233862C= , CM000681.1:g.11233862C=	GRCh37
NC_000019.8:g.11094862C=	NCBI36
NG_009060.1:g.38806C= , LRG_274:g.38806C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252444.10:c.2411C=	ENSP00000252444.6:p.Ala804=
ENST00000559340.2:c.*222C=	ENSP00000453696.2:n.*222C=
ENST00000560467.2:c.2033C=	ENSP00000453513.2:p.Ala678=
ENST00000558518.6:c.2153C= MANE Select	ENSP00000454071.1:p.Ala718=
ENST00000252444.9:c.2407C=
ENST00000455727.6:c.1649C=	ENSP00000397829.2:p.Ala550=
ENST00000535915.5:c.2030C=	ENSP00000440520.1:p.Ala677=
ENST00000545707.5:c.1619C=	ENSP00000437639.1:p.Ala540=
ENST00000557933.5:c.2153C=	ENSP00000453557.1:p.Ala718=
ENST00000558013.5:c.2153C=	ENSP00000453346.1:p.Ala718=
ENST00000558518.5:c.2153C=	ENSP00000454071.1:p.Ala718=
NM_000527.4:c.2153C= , LRG_274t1:c.2153C=	NP_000518.1:p.Ala718=
NM_001195798.1:c.2153C=	NP_001182727.1:p.Ala718=
NM_001195799.1:c.2030C=	NP_001182728.1:p.Ala677=
NM_001195800.1:c.1649C=	NP_001182729.1:p.Ala550=
NM_001195803.1:c.1619C=	NP_001182732.1:p.Ala540=
XM_011528010.1:c.2153C=	XP_011526312.1:p.Ala718=
XM_011528011.1:c.1772C=	XP_011526313.1:p.Ala591=
XR_244074.2:n.2163C=
XM_011528010.2:c.2153C=	XP_011526312.1:p.Ala718=
XR_001753685.2:n.2487C=
XR_001753686.2:n.2130C=
NM_000527.5:c.2153C= MANE Select	NP_000518.1:p.Ala718=
NM_001195798.2:c.2153C=	NP_001182727.1:p.Ala718=
NM_001195799.2:c.2030C=	NP_001182728.1:p.Ala677=
NM_001195800.2:c.1649C=	NP_001182729.1:p.Ala550=
NM_001195803.2:c.1619C=	NP_001182732.1:p.Ala540=