Canonical Allele Identifier: CA1217925890

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091026T= , CM000663.2:g.197091026T=	GRCh38
NC_000001.10:g.197060156T= , CM000663.1:g.197060156T=	GRCh37
NC_000001.9:g.195326779T=	NCBI36
NG_015867.1:g.60669A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2747A=
ENST00000367409.9:c.9460A= MANE Select	ENSP00000356379.4:p.Arg3154=
ENST00000680265.1:c.9682A=	ENSP00000505384.1:p.Arg3228=
ENST00000680710.1:c.9436A=	ENSP00000506676.1:p.Arg3146=
ENST00000294732.11:c.4705A=	ENSP00000294732.7:p.Arg1569=
ENST00000367408.5:c.2455A=	ENSP00000356378.1:p.Arg819=
ENST00000367409.8:c.9460A=	ENSP00000356379.4:p.Arg3154=
ENST00000612785.1:c.3418A=	ENSP00000479244.1:p.Arg1140=
NM_001206846.1:c.4705A=	NP_001193775.1:p.Arg1569=
NM_018136.4:c.9460A=	NP_060606.3:p.Arg3154=
NM_018136.5:c.9460A= MANE Select	NP_060606.3:p.Arg3154=
NM_001206846.2:c.4705A=	NP_001193775.1:p.Arg1569=