Canonical Allele Identifier: CA1217925840

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090978T= , CM000663.2:g.197090978T=	GRCh38
NC_000001.10:g.197060108T= , CM000663.1:g.197060108T=	GRCh37
NC_000001.9:g.195326731T=	NCBI36
NG_015867.1:g.60717A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2795A=
ENST00000367409.9:c.9508A= MANE Select	ENSP00000356379.4:p.Ile3170=
ENST00000680265.1:c.9730A=	ENSP00000505384.1:p.Ile3244=
ENST00000680710.1:c.9484A=	ENSP00000506676.1:p.Ile3162=
ENST00000294732.11:c.4753A=	ENSP00000294732.7:p.Ile1585=
ENST00000367408.5:c.2503A=	ENSP00000356378.1:p.Ile835=
ENST00000367409.8:c.9508A=	ENSP00000356379.4:p.Ile3170=
ENST00000612785.1:c.3466A=	ENSP00000479244.1:p.Ile1156=
NM_001206846.1:c.4753A=	NP_001193775.1:p.Ile1585=
NM_018136.4:c.9508A=	NP_060606.3:p.Ile3170=
NM_018136.5:c.9508A= MANE Select	NP_060606.3:p.Ile3170=
NM_001206846.2:c.4753A=	NP_001193775.1:p.Ile1585=