Canonical Allele Identifier: CA1217923607

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088417A= , CM000663.2:g.197088417A=	GRCh38
NC_000001.10:g.197057547A= , CM000663.1:g.197057547A=	GRCh37
NC_000001.9:g.195324170A=	NCBI36
NG_015867.1:g.63278T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3287T=
ENST00000367409.9:c.10000T= MANE Select	ENSP00000356379.4:p.Ser3334=
ENST00000680265.1:c.10222T=	ENSP00000505384.1:p.Ser3408=
ENST00000680710.1:c.9976T=	ENSP00000506676.1:p.Ser3326=
ENST00000294732.11:c.5245T=	ENSP00000294732.7:p.Ser1749=
ENST00000367408.5:c.2995T=	ENSP00000356378.1:p.Ser999=
ENST00000367409.8:c.10000T=	ENSP00000356379.4:p.Ser3334=
ENST00000612785.1:c.3958T=	ENSP00000479244.1:p.Ser1320=
NM_001206846.1:c.5245T=	NP_001193775.1:p.Ser1749=
NM_018136.4:c.10000T=	NP_060606.3:p.Ser3334=
NM_018136.5:c.10000T= MANE Select	NP_060606.3:p.Ser3334=
NM_001206846.2:c.5245T=	NP_001193775.1:p.Ser1749=