Canonical Allele Identifier: CA1217925669

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090862G= , CM000663.2:g.197090862G=	GRCh38
NC_000001.10:g.197059992G= , CM000663.1:g.197059992G=	GRCh37
NC_000001.9:g.195326615G=	NCBI36
NG_015867.1:g.60833C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2911C=
ENST00000367409.9:c.9624C= MANE Select	ENSP00000356379.4:p.Ile3208=
ENST00000680265.1:c.9846C=	ENSP00000505384.1:p.Ile3282=
ENST00000680710.1:c.9600C=	ENSP00000506676.1:p.Ile3200=
ENST00000294732.11:c.4869C=	ENSP00000294732.7:p.Ile1623=
ENST00000367408.5:c.2619C=	ENSP00000356378.1:p.Ile873=
ENST00000367409.8:c.9624C=	ENSP00000356379.4:p.Ile3208=
ENST00000612785.1:c.3582C=	ENSP00000479244.1:p.Ile1194=
NM_001206846.1:c.4869C=	NP_001193775.1:p.Ile1623=
NM_018136.4:c.9624C=	NP_060606.3:p.Ile3208=
NM_018136.5:c.9624C= MANE Select	NP_060606.3:p.Ile3208=
NM_001206846.2:c.4869C=	NP_001193775.1:p.Ile1623=