Canonical Allele Identifier: CA2322777169

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11123187A= , CM000681.2:g.11123187A=	GRCh38
NC_000019.9:g.11233863A= , CM000681.1:g.11233863A=	GRCh37
NC_000019.8:g.11094863A=	NCBI36
NG_009060.1:g.38807A= , LRG_274:g.38807A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2412A=	ENSP00000252444.6:p.Ala804=
ENST00000559340.2:c.*223A=	ENSP00000453696.2:n.*223A=
ENST00000560467.2:c.2034A=	ENSP00000453513.2:p.Ala678=
ENST00000558518.6:c.2154A= MANE Select	ENSP00000454071.1:p.Ala718=
ENST00000252444.9:c.2408A=
ENST00000455727.6:c.1650A=	ENSP00000397829.2:p.Ala550=
ENST00000535915.5:c.2031A=	ENSP00000440520.1:p.Ala677=
ENST00000545707.5:c.1620A=	ENSP00000437639.1:p.Ala540=
ENST00000557933.5:c.2154A=	ENSP00000453557.1:p.Ala718=
ENST00000558013.5:c.2154A=	ENSP00000453346.1:p.Ala718=
ENST00000558518.5:c.2154A=	ENSP00000454071.1:p.Ala718=
NM_000527.4:c.2154A= , LRG_274t1:c.2154A=	NP_000518.1:p.Ala718=
NM_001195798.1:c.2154A=	NP_001182727.1:p.Ala718=
NM_001195799.1:c.2031A=	NP_001182728.1:p.Ala677=
NM_001195800.1:c.1650A=	NP_001182729.1:p.Ala550=
NM_001195803.1:c.1620A=	NP_001182732.1:p.Ala540=
XM_011528010.1:c.2154A=	XP_011526312.1:p.Ala718=
XM_011528011.1:c.1773A=	XP_011526313.1:p.Ala591=
XR_244074.2:n.2164A=
XM_011528010.2:c.2154A=	XP_011526312.1:p.Ala718=
XR_001753685.2:n.2488A=
XR_001753686.2:n.2131A=
NM_000527.5:c.2154A= MANE Select	NP_000518.1:p.Ala718=
NM_001195798.2:c.2154A=	NP_001182727.1:p.Ala718=
NM_001195799.2:c.2031A=	NP_001182728.1:p.Ala677=
NM_001195800.2:c.1650A=	NP_001182729.1:p.Ala550=
NM_001195803.2:c.1620A=	NP_001182732.1:p.Ala540=