Canonical Allele Identifier: CA1217925120

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090196C= , CM000663.2:g.197090196C=	GRCh38
NC_000001.10:g.197059326C= , CM000663.1:g.197059326C=	GRCh37
NC_000001.9:g.195325949C=	NCBI36
NG_015867.1:g.61499G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3116G=
ENST00000367409.9:c.9829G= MANE Select	ENSP00000356379.4:p.Glu3277=
ENST00000680265.1:c.10051G=	ENSP00000505384.1:p.Glu3351=
ENST00000680710.1:c.9805G=	ENSP00000506676.1:p.Glu3269=
ENST00000294732.11:c.5074G=	ENSP00000294732.7:p.Glu1692=
ENST00000367408.5:c.2824G=	ENSP00000356378.1:p.Glu942=
ENST00000367409.8:c.9829G=	ENSP00000356379.4:p.Glu3277=
ENST00000612785.1:c.3787G=	ENSP00000479244.1:p.Glu1263=
NM_001206846.1:c.5074G=	NP_001193775.1:p.Glu1692=
NM_018136.4:c.9829G=	NP_060606.3:p.Glu3277=
NM_018136.5:c.9829G= MANE Select	NP_060606.3:p.Glu3277=
NM_001206846.2:c.5074G=	NP_001193775.1:p.Glu1692=