Canonical Allele Identifier: CA1217923602

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088411C= , CM000663.2:g.197088411C=	GRCh38
NC_000001.10:g.197057541C= , CM000663.1:g.197057541C=	GRCh37
NC_000001.9:g.195324164C=	NCBI36
NG_015867.1:g.63284G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3293G=
ENST00000367409.9:c.10006G= MANE Select	ENSP00000356379.4:p.Val3336=
ENST00000680265.1:c.10228G=	ENSP00000505384.1:p.Val3410=
ENST00000680710.1:c.9982G=	ENSP00000506676.1:p.Val3328=
ENST00000294732.11:c.5251G=	ENSP00000294732.7:p.Val1751=
ENST00000367408.5:c.3001G=	ENSP00000356378.1:p.Val1001=
ENST00000367409.8:c.10006G=	ENSP00000356379.4:p.Val3336=
ENST00000612785.1:c.3964G=	ENSP00000479244.1:p.Val1322=
NM_001206846.1:c.5251G=	NP_001193775.1:p.Val1751=
NM_018136.4:c.10006G=	NP_060606.3:p.Val3336=
NM_018136.5:c.10006G= MANE Select	NP_060606.3:p.Val3336=
NM_001206846.2:c.5251G=	NP_001193775.1:p.Val1751=