Canonical Allele Identifier: CA1217923597

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088404T= , CM000663.2:g.197088404T=	GRCh38
NC_000001.10:g.197057534T= , CM000663.1:g.197057534T=	GRCh37
NC_000001.9:g.195324157T=	NCBI36
NG_015867.1:g.63291A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3300A=
ENST00000367409.9:c.10013A= MANE Select	ENSP00000356379.4:p.Asp3338=
ENST00000680265.1:c.10235A=	ENSP00000505384.1:p.Asp3412=
ENST00000680710.1:c.9989A=	ENSP00000506676.1:p.Asp3330=
ENST00000294732.11:c.5258A=	ENSP00000294732.7:p.Asp1753=
ENST00000367408.5:c.3008A=	ENSP00000356378.1:p.Asp1003=
ENST00000367409.8:c.10013A=	ENSP00000356379.4:p.Asp3338=
ENST00000612785.1:c.3971A=	ENSP00000479244.1:p.Asp1324=
NM_001206846.1:c.5258A=	NP_001193775.1:p.Asp1753=
NM_018136.4:c.10013A=	NP_060606.3:p.Asp3338=
NM_018136.5:c.10013A= MANE Select	NP_060606.3:p.Asp3338=
NM_001206846.2:c.5258A=	NP_001193775.1:p.Asp1753=