Canonical Allele Identifier: CA1217926676

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093075G= , CM000663.2:g.197093075G=	GRCh38
NC_000001.10:g.197062205G= , CM000663.1:g.197062205G=	GRCh37
NC_000001.9:g.195328828G=	NCBI36
NG_015867.1:g.58620C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2558C=
ENST00000367409.9:c.9271C= MANE Select	ENSP00000356379.4:p.Arg3091=
ENST00000680265.1:c.9493C=	ENSP00000505384.1:p.Arg3165=
ENST00000680710.1:c.9271C=	ENSP00000506676.1:p.Arg3091=
ENST00000294732.11:c.4516C=	ENSP00000294732.7:p.Arg1506=
ENST00000367408.5:c.2266C=	ENSP00000356378.1:p.Arg756=
ENST00000367409.8:c.9271C=	ENSP00000356379.4:p.Arg3091=
ENST00000612785.1:c.3229C=	ENSP00000479244.1:p.Arg1077=
NM_001206846.1:c.4516C=	NP_001193775.1:p.Arg1506=
NM_018136.4:c.9271C=	NP_060606.3:p.Arg3091=
NM_018136.5:c.9271C= MANE Select	NP_060606.3:p.Arg3091=
NM_001206846.2:c.4516C=	NP_001193775.1:p.Arg1506=