Canonical Allele Identifier: CA1143737097

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197102962C= , CM000663.2:g.197102962C=	GRCh38
NC_000001.10:g.197072092C= , CM000663.1:g.197072092C=	GRCh37
NC_000001.9:g.195338715C=	NCBI36
NG_015867.1:g.48733G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-6798G=
ENST00000367409.9:c.6289G= MANE Select	ENSP00000356379.4:p.Ala2097=
ENST00000680265.1:c.6289G=	ENSP00000505384.1:p.Ala2097=
ENST00000680710.1:c.6289G=	ENSP00000506676.1:p.Ala2097=
ENST00000294732.11:c.4066-6798G=	ENSP00000294732.7:n.4066-6798G=
ENST00000367408.5:c.1816-6798G=	ENSP00000356378.1:n.1816-6798G=
ENST00000367409.8:c.6289G=	ENSP00000356379.4:p.Ala2097=
ENST00000612785.1:c.562-315G=	ENSP00000479244.1:n.562-315G=
NM_001206846.1:c.4066-6798G=	NP_001193775.1:n.4066-6798G=
NM_018136.4:c.6289G=	NP_060606.3:p.Ala2097=
NM_018136.5:c.6289G= MANE Select	NP_060606.3:p.Ala2097=
NM_001206846.2:c.4066-6798G=	NP_001193775.1:n.4066-6798G=