Canonical Allele Identifier: CA1217931173

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197104747G= , CM000663.2:g.197104747G=	GRCh38
NC_000001.10:g.197073877G= , CM000663.1:g.197073877G=	GRCh37
NC_000001.9:g.195340500G=	NCBI36
NG_015867.1:g.46948C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2108-8583C=
ENST00000367409.9:c.4504C= MANE Select	ENSP00000356379.4:p.Gln1502=
ENST00000680265.1:c.4504C=	ENSP00000505384.1:p.Gln1502=
ENST00000680710.1:c.4504C=	ENSP00000506676.1:p.Gln1502=
ENST00000681879.1:c.4552C=	ENSP00000505363.1:n.4552C=
ENST00000294732.11:c.4066-8583C=	ENSP00000294732.7:n.4066-8583C=
ENST00000367408.5:c.1816-8583C=	ENSP00000356378.1:n.1816-8583C=
ENST00000367409.8:c.4504C=	ENSP00000356379.4:p.Gln1502=
ENST00000612785.1:c.562-2100C=	ENSP00000479244.1:n.562-2100C=
NM_001206846.1:c.4066-8583C=	NP_001193775.1:n.4066-8583C=
NM_018136.4:c.4504C=	NP_060606.3:p.Gln1502=
NM_018136.5:c.4504C= MANE Select	NP_060606.3:p.Gln1502=
NM_001206846.2:c.4066-8583C=	NP_001193775.1:n.4066-8583C=