Canonical Allele Identifier: CA1148349526

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090965C= , CM000663.2:g.197090965C=	GRCh38
NC_000001.10:g.197060095C= , CM000663.1:g.197060095C=	GRCh37
NC_000001.9:g.195326718C=	NCBI36
NG_015867.1:g.60730G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2808G=
ENST00000367409.9:c.9521G= MANE Select	ENSP00000356379.4:p.Gly3174=
ENST00000680265.1:c.9743G=	ENSP00000505384.1:p.Gly3248=
ENST00000680710.1:c.9497G=	ENSP00000506676.1:p.Gly3166=
ENST00000294732.11:c.4766G=	ENSP00000294732.7:p.Gly1589=
ENST00000367408.5:c.2516G=	ENSP00000356378.1:p.Gly839=
ENST00000367409.8:c.9521G=	ENSP00000356379.4:p.Gly3174=
ENST00000612785.1:c.3479G=	ENSP00000479244.1:p.Gly1160=
NM_001206846.1:c.4766G=	NP_001193775.1:p.Gly1589=
NM_018136.4:c.9521G=	NP_060606.3:p.Gly3174=
NM_018136.5:c.9521G= MANE Select	NP_060606.3:p.Gly3174=
NM_001206846.2:c.4766G=	NP_001193775.1:p.Gly1589=