Canonical Allele Identifier: CA1217925834

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090966C= , CM000663.2:g.197090966C=	GRCh38
NC_000001.10:g.197060096C= , CM000663.1:g.197060096C=	GRCh37
NC_000001.9:g.195326719C=	NCBI36
NG_015867.1:g.60729G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2807G=
ENST00000367409.9:c.9520G= MANE Select	ENSP00000356379.4:p.Gly3174=
ENST00000680265.1:c.9742G=	ENSP00000505384.1:p.Gly3248=
ENST00000680710.1:c.9496G=	ENSP00000506676.1:p.Gly3166=
ENST00000294732.11:c.4765G=	ENSP00000294732.7:p.Gly1589=
ENST00000367408.5:c.2515G=	ENSP00000356378.1:p.Gly839=
ENST00000367409.8:c.9520G=	ENSP00000356379.4:p.Gly3174=
ENST00000612785.1:c.3478G=	ENSP00000479244.1:p.Gly1160=
NM_001206846.1:c.4765G=	NP_001193775.1:p.Gly1589=
NM_018136.4:c.9520G=	NP_060606.3:p.Gly3174=
NM_018136.5:c.9520G= MANE Select	NP_060606.3:p.Gly3174=
NM_001206846.2:c.4765G=	NP_001193775.1:p.Gly1589=