Canonical Allele Identifier: CA1217925864

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091004A= , CM000663.2:g.197091004A=	GRCh38
NC_000001.10:g.197060134A= , CM000663.1:g.197060134A=	GRCh37
NC_000001.9:g.195326757A=	NCBI36
NG_015867.1:g.60691T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2769T=
ENST00000367409.9:c.9482T= MANE Select	ENSP00000356379.4:p.Ile3161=
ENST00000680265.1:c.9704T=	ENSP00000505384.1:p.Ile3235=
ENST00000680710.1:c.9458T=	ENSP00000506676.1:p.Ile3153=
ENST00000294732.11:c.4727T=	ENSP00000294732.7:p.Ile1576=
ENST00000367408.5:c.2477T=	ENSP00000356378.1:p.Ile826=
ENST00000367409.8:c.9482T=	ENSP00000356379.4:p.Ile3161=
ENST00000612785.1:c.3440T=	ENSP00000479244.1:p.Ile1147=
NM_001206846.1:c.4727T=	NP_001193775.1:p.Ile1576=
NM_018136.4:c.9482T=	NP_060606.3:p.Ile3161=
NM_018136.5:c.9482T= MANE Select	NP_060606.3:p.Ile3161=
NM_001206846.2:c.4727T=	NP_001193775.1:p.Ile1576=