Canonical Allele Identifier: CA1146263202

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088599T= , CM000663.2:g.197088599T=	GRCh38
NC_000001.10:g.197057729T= , CM000663.1:g.197057729T=	GRCh37
NC_000001.9:g.195324352T=	NCBI36
NG_015867.1:g.63096A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3272-167A=
ENST00000367409.9:c.9985-167A= MANE Select	ENSP00000356379.4:n.9985-167A=
ENST00000680265.1:c.10207-167A=	ENSP00000505384.1:n.10207-167A=
ENST00000680710.1:c.9961-167A=	ENSP00000506676.1:n.9961-167A=
ENST00000294732.11:c.5230-167A=	ENSP00000294732.7:n.5230-167A=
ENST00000367408.5:c.2980-167A=	ENSP00000356378.1:n.2980-167A=
ENST00000367409.8:c.9985-167A=	ENSP00000356379.4:n.9985-167A=
ENST00000612785.1:c.3943-167A=	ENSP00000479244.1:n.3943-167A=
NM_001206846.1:c.5230-167A=	NP_001193775.1:n.5230-167A=
NM_018136.4:c.9985-167A=	NP_060606.3:n.9985-167A=
NM_018136.5:c.9985-167A= MANE Select	NP_060606.3:n.9985-167A=
NM_001206846.2:c.5230-167A=	NP_001193775.1:n.5230-167A=