Canonical Allele Identifier: CA1217926703

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093159T= , CM000663.2:g.197093159T=	GRCh38
NC_000001.10:g.197062289T= , CM000663.1:g.197062289T=	GRCh37
NC_000001.9:g.195328912T=	NCBI36
NG_015867.1:g.58536A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2474A=
ENST00000367409.9:c.9187A= MANE Select	ENSP00000356379.4:p.Ile3063=
ENST00000680265.1:c.9409A=	ENSP00000505384.1:p.Ile3137=
ENST00000680710.1:c.9187A=	ENSP00000506676.1:p.Ile3063=
ENST00000294732.11:c.4432A=	ENSP00000294732.7:p.Ile1478=
ENST00000367408.5:c.2182A=	ENSP00000356378.1:p.Ile728=
ENST00000367409.8:c.9187A=	ENSP00000356379.4:p.Ile3063=
ENST00000612785.1:c.3145A=	ENSP00000479244.1:p.Ile1049=
NM_001206846.1:c.4432A=	NP_001193775.1:p.Ile1478=
NM_018136.4:c.9187A=	NP_060606.3:p.Ile3063=
NM_018136.5:c.9187A= MANE Select	NP_060606.3:p.Ile3063=
NM_001206846.2:c.4432A=	NP_001193775.1:p.Ile1478=