Canonical Allele Identifier: CA1217925872

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091015T= , CM000663.2:g.197091015T=	GRCh38
NC_000001.10:g.197060145T= , CM000663.1:g.197060145T=	GRCh37
NC_000001.9:g.195326768T=	NCBI36
NG_015867.1:g.60680A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2758A=
ENST00000367409.9:c.9471A= MANE Select	ENSP00000356379.4:p.Glu3157=
ENST00000680265.1:c.9693A=	ENSP00000505384.1:p.Glu3231=
ENST00000680710.1:c.9447A=	ENSP00000506676.1:p.Glu3149=
ENST00000294732.11:c.4716A=	ENSP00000294732.7:p.Glu1572=
ENST00000367408.5:c.2466A=	ENSP00000356378.1:p.Glu822=
ENST00000367409.8:c.9471A=	ENSP00000356379.4:p.Glu3157=
ENST00000612785.1:c.3429A=	ENSP00000479244.1:p.Glu1143=
NM_001206846.1:c.4716A=	NP_001193775.1:p.Glu1572=
NM_018136.4:c.9471A=	NP_060606.3:p.Glu3157=
NM_018136.5:c.9471A= MANE Select	NP_060606.3:p.Glu3157=
NM_001206846.2:c.4716A=	NP_001193775.1:p.Glu1572=