Canonical Allele Identifier: CA1149121290

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093208C= , CM000663.2:g.197093208C=	GRCh38
NC_000001.10:g.197062338C= , CM000663.1:g.197062338C=	GRCh37
NC_000001.9:g.195328961C=	NCBI36
NG_015867.1:g.58487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2425G=
ENST00000367409.9:c.9138G= MANE Select	ENSP00000356379.4:p.Arg3046=
ENST00000680265.1:c.9360G=	ENSP00000505384.1:p.Arg3120=
ENST00000680710.1:c.9138G=	ENSP00000506676.1:p.Arg3046=
ENST00000294732.11:c.4383G=	ENSP00000294732.7:p.Arg1461=
ENST00000367408.5:c.2133G=	ENSP00000356378.1:p.Arg711=
ENST00000367409.8:c.9138G=	ENSP00000356379.4:p.Arg3046=
ENST00000612785.1:c.3096G=	ENSP00000479244.1:p.Arg1032=
NM_001206846.1:c.4383G=	NP_001193775.1:p.Arg1461=
NM_018136.4:c.9138G=	NP_060606.3:p.Arg3046=
NM_018136.5:c.9138G= MANE Select	NP_060606.3:p.Arg3046=
NM_001206846.2:c.4383G=	NP_001193775.1:p.Arg1461=