Canonical Allele Identifier: CA1217925136

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090218A= , CM000663.2:g.197090218A=	GRCh38
NC_000001.10:g.197059348A= , CM000663.1:g.197059348A=	GRCh37
NC_000001.9:g.195325971A=	NCBI36
NG_015867.1:g.61477T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3094T=
ENST00000367409.9:c.9807T= MANE Select	ENSP00000356379.4:p.Ile3269=
ENST00000680265.1:c.10029T=	ENSP00000505384.1:p.Ile3343=
ENST00000680710.1:c.9783T=	ENSP00000506676.1:p.Ile3261=
ENST00000294732.11:c.5052T=	ENSP00000294732.7:p.Ile1684=
ENST00000367408.5:c.2802T=	ENSP00000356378.1:p.Ile934=
ENST00000367409.8:c.9807T=	ENSP00000356379.4:p.Ile3269=
ENST00000612785.1:c.3765T=	ENSP00000479244.1:p.Ile1255=
NM_001206846.1:c.5052T=	NP_001193775.1:p.Ile1684=
NM_018136.4:c.9807T=	NP_060606.3:p.Ile3269=
NM_018136.5:c.9807T= MANE Select	NP_060606.3:p.Ile3269=
NM_001206846.2:c.5052T=	NP_001193775.1:p.Ile1684=