Canonical Allele Identifier: CA1217923611

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088420T= , CM000663.2:g.197088420T=	GRCh38
NC_000001.10:g.197057550T= , CM000663.1:g.197057550T=	GRCh37
NC_000001.9:g.195324173T=	NCBI36
NG_015867.1:g.63275A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3284A=
ENST00000367409.9:c.9997A= MANE Select	ENSP00000356379.4:p.Thr3333=
ENST00000680265.1:c.10219A=	ENSP00000505384.1:p.Thr3407=
ENST00000680710.1:c.9973A=	ENSP00000506676.1:p.Thr3325=
ENST00000294732.11:c.5242A=	ENSP00000294732.7:p.Thr1748=
ENST00000367408.5:c.2992A=	ENSP00000356378.1:p.Thr998=
ENST00000367409.8:c.9997A=	ENSP00000356379.4:p.Thr3333=
ENST00000612785.1:c.3955A=	ENSP00000479244.1:p.Thr1319=
NM_001206846.1:c.5242A=	NP_001193775.1:p.Thr1748=
NM_018136.4:c.9997A=	NP_060606.3:p.Thr3333=
NM_018136.5:c.9997A= MANE Select	NP_060606.3:p.Thr3333=
NM_001206846.2:c.5242A=	NP_001193775.1:p.Thr1748=