Canonical Allele Identifier: CA1217925827

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090963G= , CM000663.2:g.197090963G=	GRCh38
NC_000001.10:g.197060093G= , CM000663.1:g.197060093G=	GRCh37
NC_000001.9:g.195326716G=	NCBI36
NG_015867.1:g.60732C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2810C=
ENST00000367409.9:c.9523C= MANE Select	ENSP00000356379.4:p.Gln3175=
ENST00000680265.1:c.9745C=	ENSP00000505384.1:p.Gln3249=
ENST00000680710.1:c.9499C=	ENSP00000506676.1:p.Gln3167=
ENST00000294732.11:c.4768C=	ENSP00000294732.7:p.Gln1590=
ENST00000367408.5:c.2518C=	ENSP00000356378.1:p.Gln840=
ENST00000367409.8:c.9523C=	ENSP00000356379.4:p.Gln3175=
ENST00000612785.1:c.3481C=	ENSP00000479244.1:p.Gln1161=
NM_001206846.1:c.4768C=	NP_001193775.1:p.Gln1590=
NM_018136.4:c.9523C=	NP_060606.3:p.Gln3175=
NM_018136.5:c.9523C= MANE Select	NP_060606.3:p.Gln3175=
NM_001206846.2:c.4768C=	NP_001193775.1:p.Gln1590=