Canonical Allele Identifier: CA2322775635

Gene: LDLR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.11120481A= , CM000681.2:g.11120481A=	GRCh38
NC_000019.9:g.11231157A= , CM000681.1:g.11231157A=	GRCh37
NC_000019.8:g.11092157A=	NCBI36
NG_009060.1:g.36101A= , LRG_274:g.36101A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252444.10:c.2357A=	ENSP00000252444.6:p.Asp786=
ENST00000559340.2:c.*168A=	ENSP00000453696.2:n.*168A=
ENST00000560467.2:c.1979A=	ENSP00000453513.2:p.Asp660=
ENST00000558518.6:c.2099A= MANE Select	ENSP00000454071.1:p.Asp700=
ENST00000252444.9:c.2353A=
ENST00000455727.6:c.1595A=	ENSP00000397829.2:p.Asp532=
ENST00000535915.5:c.1976A=	ENSP00000440520.1:p.Asp659=
ENST00000545707.5:c.1606+248A=	ENSP00000437639.1:n.1606+248A=
ENST00000557933.5:c.2099A=	ENSP00000453557.1:p.Asp700=
ENST00000558013.5:c.2099A=	ENSP00000453346.1:p.Asp700=
ENST00000558518.5:c.2099A=	ENSP00000454071.1:p.Asp700=
NM_000527.4:c.2099A= , LRG_274t1:c.2099A=	NP_000518.1:p.Asp700=
NM_001195798.1:c.2099A=	NP_001182727.1:p.Asp700=
NM_001195799.1:c.1976A=	NP_001182728.1:p.Asp659=
NM_001195800.1:c.1595A=	NP_001182729.1:p.Asp532=
NM_001195803.1:c.1606+248A=	NP_001182732.1:n.1606+248A=
XM_011528010.1:c.2099A=	XP_011526312.1:p.Asp700=
XM_011528011.1:c.1718A=	XP_011526313.1:p.Asp573=
XR_244074.2:n.2109A=
XM_011528010.2:c.2099A=	XP_011526312.1:p.Asp700=
XR_001753685.2:n.2216A=
XR_001753686.2:n.2076A=
NM_000527.5:c.2099A= MANE Select	NP_000518.1:p.Asp700=
NM_001195798.2:c.2099A=	NP_001182727.1:p.Asp700=
NM_001195799.2:c.1976A=	NP_001182728.1:p.Asp659=
NM_001195800.2:c.1595A=	NP_001182729.1:p.Asp532=
NM_001195803.2:c.1606+248A=	NP_001182732.1:n.1606+248A=