Canonical Allele Identifier: CA1217925166

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090249T= , CM000663.2:g.197090249T=	GRCh38
NC_000001.10:g.197059379T= , CM000663.1:g.197059379T=	GRCh37
NC_000001.9:g.195326002T=	NCBI36
NG_015867.1:g.61446A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3063A=
ENST00000367409.9:c.9776A= MANE Select	ENSP00000356379.4:p.Tyr3259=
ENST00000680265.1:c.9998A=	ENSP00000505384.1:p.Tyr3333=
ENST00000680710.1:c.9752A=	ENSP00000506676.1:p.Tyr3251=
ENST00000294732.11:c.5021A=	ENSP00000294732.7:p.Tyr1674=
ENST00000367408.5:c.2771A=	ENSP00000356378.1:p.Tyr924=
ENST00000367409.8:c.9776A=	ENSP00000356379.4:p.Tyr3259=
ENST00000612785.1:c.3734A=	ENSP00000479244.1:p.Tyr1245=
NM_001206846.1:c.5021A=	NP_001193775.1:p.Tyr1674=
NM_018136.4:c.9776A=	NP_060606.3:p.Tyr3259=
NM_018136.5:c.9776A= MANE Select	NP_060606.3:p.Tyr3259=
NM_001206846.2:c.5021A=	NP_001193775.1:p.Tyr1674=