Canonical Allele Identifier: CA1217936839

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117901G= , CM000663.2:g.197117901G=	GRCh38
NC_000001.10:g.197087031G= , CM000663.1:g.197087031G=	GRCh37
NC_000001.9:g.195353654G=	NCBI36
NG_015867.1:g.33794C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.1995C=
ENST00000367409.9:c.3953C= MANE Select	ENSP00000356379.4:p.Ala1318=
ENST00000680265.1:c.3953C=	ENSP00000505384.1:p.Ala1318=
ENST00000680710.1:c.3953C=	ENSP00000506676.1:p.Ala1318=
ENST00000681879.1:c.4001C=	ENSP00000505363.1:n.4001C=
ENST00000294732.11:c.3953C=	ENSP00000294732.7:p.Ala1318=
ENST00000367408.5:c.1703C=	ENSP00000356378.1:p.Ala568=
ENST00000367409.8:c.3953C=	ENSP00000356379.4:p.Ala1318=
ENST00000612785.1:c.562-15254C=	ENSP00000479244.1:n.562-15254C=
NM_001206846.1:c.3953C=	NP_001193775.1:p.Ala1318=
NM_018136.4:c.3953C=	NP_060606.3:p.Ala1318=
NM_018136.5:c.3953C= MANE Select	NP_060606.3:p.Ala1318=
NM_001206846.2:c.3953C=	NP_001193775.1:p.Ala1318=