Canonical Allele Identifier: CA1217926667

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093060G= , CM000663.2:g.197093060G=	GRCh38
NC_000001.10:g.197062190G= , CM000663.1:g.197062190G=	GRCh37
NC_000001.9:g.195328813G=	NCBI36
NG_015867.1:g.58635C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2573C=
ENST00000367409.9:c.9286C= MANE Select	ENSP00000356379.4:p.Arg3096=
ENST00000680265.1:c.9508C=	ENSP00000505384.1:p.Arg3170=
ENST00000680710.1:c.9286C=	ENSP00000506676.1:p.Arg3096=
ENST00000294732.11:c.4531C=	ENSP00000294732.7:p.Arg1511=
ENST00000367408.5:c.2281C=	ENSP00000356378.1:p.Arg761=
ENST00000367409.8:c.9286C=	ENSP00000356379.4:p.Arg3096=
ENST00000612785.1:c.3244C=	ENSP00000479244.1:p.Arg1082=
NM_001206846.1:c.4531C=	NP_001193775.1:p.Arg1511=
NM_018136.4:c.9286C=	NP_060606.3:p.Arg3096=
NM_018136.5:c.9286C= MANE Select	NP_060606.3:p.Arg3096=
NM_001206846.2:c.4531C=	NP_001193775.1:p.Arg1511=