Canonical Allele Identifier: CA1217925345

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090380C= , CM000663.2:g.197090380C=	GRCh38
NC_000001.10:g.197059510C= , CM000663.1:g.197059510C=	GRCh37
NC_000001.9:g.195326133C=	NCBI36
NG_015867.1:g.61315G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2932G=
ENST00000367409.9:c.9645G= MANE Select	ENSP00000356379.4:p.Trp3215=
ENST00000680265.1:c.9867G=	ENSP00000505384.1:p.Trp3289=
ENST00000680710.1:c.9621G=	ENSP00000506676.1:p.Trp3207=
ENST00000294732.11:c.4890G=	ENSP00000294732.7:p.Trp1630=
ENST00000367408.5:c.2640G=	ENSP00000356378.1:p.Trp880=
ENST00000367409.8:c.9645G=	ENSP00000356379.4:p.Trp3215=
ENST00000612785.1:c.3603G=	ENSP00000479244.1:p.Trp1201=
NM_001206846.1:c.4890G=	NP_001193775.1:p.Trp1630=
NM_018136.4:c.9645G=	NP_060606.3:p.Trp3215=
NM_018136.5:c.9645G= MANE Select	NP_060606.3:p.Trp3215=
NM_001206846.2:c.4890G=	NP_001193775.1:p.Trp1630=