Canonical Allele Identifier: CA1217930314

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102484C= , CM000663.2:g.197102484C=	GRCh38
NC_000001.10:g.197071614C= , CM000663.1:g.197071614C=	GRCh37
NC_000001.9:g.195338237C=	NCBI36
NG_015867.1:g.49211G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6320G=
ENST00000367409.9:c.6767G= MANE Select	ENSP00000356379.4:p.Arg2256=
ENST00000680265.1:c.6767G=	ENSP00000505384.1:p.Arg2256=
ENST00000680710.1:c.6767G=	ENSP00000506676.1:p.Arg2256=
ENST00000294732.11:c.4066-6320G=	ENSP00000294732.7:n.4066-6320G=
ENST00000367408.5:c.1816-6320G=	ENSP00000356378.1:n.1816-6320G=
ENST00000367409.8:c.6767G=	ENSP00000356379.4:p.Arg2256=
ENST00000612785.1:c.725G=	ENSP00000479244.1:p.Arg242=
NM_001206846.1:c.4066-6320G=	NP_001193775.1:n.4066-6320G=
NM_018136.4:c.6767G=	NP_060606.3:p.Arg2256=
NM_018136.5:c.6767G= MANE Select	NP_060606.3:p.Arg2256=
NM_001206846.2:c.4066-6320G=	NP_001193775.1:n.4066-6320G=