Canonical Allele Identifier: CA1143678817

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117798T= , CM000663.2:g.197117798T=	GRCh38
NC_000001.10:g.197086928T= , CM000663.1:g.197086928T=	GRCh37
NC_000001.9:g.195353551T=	NCBI36
NG_015867.1:g.33897A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2098A=
ENST00000367409.9:c.4056A= MANE Select	ENSP00000356379.4:p.Ser1352=
ENST00000680265.1:c.4056A=	ENSP00000505384.1:p.Ser1352=
ENST00000680710.1:c.4056A=	ENSP00000506676.1:p.Ser1352=
ENST00000681879.1:c.4104A=	ENSP00000505363.1:n.4104A=
ENST00000294732.11:c.4056A=	ENSP00000294732.7:p.Ser1352=
ENST00000367408.5:c.1806A=	ENSP00000356378.1:p.Ser602=
ENST00000367409.8:c.4056A=	ENSP00000356379.4:p.Ser1352=
ENST00000612785.1:c.562-15151A=	ENSP00000479244.1:n.562-15151A=
NM_001206846.1:c.4056A=	NP_001193775.1:p.Ser1352=
NM_018136.4:c.4056A=	NP_060606.3:p.Ser1352=
NM_018136.5:c.4056A= MANE Select	NP_060606.3:p.Ser1352=
NM_001206846.2:c.4056A=	NP_001193775.1:p.Ser1352=