Canonical Allele Identifier: CA1217923494

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088287G= , CM000663.2:g.197088287G=	GRCh38
NC_000001.10:g.197057417G= , CM000663.1:g.197057417G=	GRCh37
NC_000001.9:g.195324040G=	NCBI36
NG_015867.1:g.63408C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3417C=
ENST00000367409.9:c.10130C= MANE Select	ENSP00000356379.4:p.Ala3377=
ENST00000680265.1:c.10352C=	ENSP00000505384.1:p.Ala3451=
ENST00000680710.1:c.10106C=	ENSP00000506676.1:p.Ala3369=
ENST00000294732.11:c.5375C=	ENSP00000294732.7:p.Ala1792=
ENST00000367408.5:c.3125C=	ENSP00000356378.1:p.Ala1042=
ENST00000367409.8:c.10130C=	ENSP00000356379.4:p.Ala3377=
ENST00000612785.1:c.4088C=	ENSP00000479244.1:p.Ala1363=
NM_001206846.1:c.5375C=	NP_001193775.1:p.Ala1792=
NM_018136.4:c.10130C=	NP_060606.3:p.Ala3377=
NM_018136.5:c.10130C= MANE Select	NP_060606.3:p.Ala3377=
NM_001206846.2:c.5375C=	NP_001193775.1:p.Ala1792=