Canonical Allele Identifier: CA1217926689

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093117T= , CM000663.2:g.197093117T=	GRCh38
NC_000001.10:g.197062247T= , CM000663.1:g.197062247T=	GRCh37
NC_000001.9:g.195328870T=	NCBI36
NG_015867.1:g.58578A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2516A=
ENST00000367409.9:c.9229A= MANE Select	ENSP00000356379.4:p.Ile3077=
ENST00000680265.1:c.9451A=	ENSP00000505384.1:p.Ile3151=
ENST00000680710.1:c.9229A=	ENSP00000506676.1:p.Ile3077=
ENST00000294732.11:c.4474A=	ENSP00000294732.7:p.Ile1492=
ENST00000367408.5:c.2224A=	ENSP00000356378.1:p.Ile742=
ENST00000367409.8:c.9229A=	ENSP00000356379.4:p.Ile3077=
ENST00000612785.1:c.3187A=	ENSP00000479244.1:p.Ile1063=
NM_001206846.1:c.4474A=	NP_001193775.1:p.Ile1492=
NM_018136.4:c.9229A=	NP_060606.3:p.Ile3077=
NM_018136.5:c.9229A= MANE Select	NP_060606.3:p.Ile3077=
NM_001206846.2:c.4474A=	NP_001193775.1:p.Ile1492=