Canonical Allele Identifier: CA1217926697

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093144C= , CM000663.2:g.197093144C=	GRCh38
NC_000001.10:g.197062274C= , CM000663.1:g.197062274C=	GRCh37
NC_000001.9:g.195328897C=	NCBI36
NG_015867.1:g.58551G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2489G=
ENST00000367409.9:c.9202G= MANE Select	ENSP00000356379.4:p.Ala3068=
ENST00000680265.1:c.9424G=	ENSP00000505384.1:p.Ala3142=
ENST00000680710.1:c.9202G=	ENSP00000506676.1:p.Ala3068=
ENST00000294732.11:c.4447G=	ENSP00000294732.7:p.Ala1483=
ENST00000367408.5:c.2197G=	ENSP00000356378.1:p.Ala733=
ENST00000367409.8:c.9202G=	ENSP00000356379.4:p.Ala3068=
ENST00000612785.1:c.3160G=	ENSP00000479244.1:p.Ala1054=
NM_001206846.1:c.4447G=	NP_001193775.1:p.Ala1483=
NM_018136.4:c.9202G=	NP_060606.3:p.Ala3068=
NM_018136.5:c.9202G= MANE Select	NP_060606.3:p.Ala3068=
NM_001206846.2:c.4447G=	NP_001193775.1:p.Ala1483=