Canonical Allele Identifier: CA1217941144

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197128717A= , CM000663.2:g.197128717A=	GRCh38
NC_000001.10:g.197097847A= , CM000663.1:g.197097847A=	GRCh37
NC_000001.9:g.195364470A=	NCBI36
NG_015867.1:g.22978T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.661T=
ENST00000367409.9:c.2761-52T= MANE Select	ENSP00000356379.4:n.2761-52T=
ENST00000680112.1:n.817-52T=
ENST00000680265.1:c.2761-52T=	ENSP00000505384.1:n.2761-52T=
ENST00000680710.1:c.2761-52T=	ENSP00000506676.1:n.2761-52T=
ENST00000681879.1:c.2761-52T=	ENSP00000505363.1:n.2761-52T=
ENST00000294732.11:c.2761-52T=	ENSP00000294732.7:n.2761-52T=
ENST00000367408.5:c.511-52T=	ENSP00000356378.1:n.511-52T=
ENST00000367409.8:c.2761-52T=	ENSP00000356379.4:n.2761-52T=
ENST00000612785.1:c.561+14974T=	ENSP00000479244.1:n.561+14974T=
NM_001206846.1:c.2761-52T=	NP_001193775.1:n.2761-52T=
NM_018136.4:c.2761-52T=	NP_060606.3:n.2761-52T=
NM_018136.5:c.2761-52T= MANE Select	NP_060606.3:n.2761-52T=
NM_001206846.2:c.2761-52T=	NP_001193775.1:n.2761-52T=