Canonical Allele Identifier: CA1217925373

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090409T= , CM000663.2:g.197090409T=	GRCh38
NC_000001.10:g.197059539T= , CM000663.1:g.197059539T=	GRCh37
NC_000001.9:g.195326162T=	NCBI36
NG_015867.1:g.61286A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2924-21A=
ENST00000367409.9:c.9637-21A= MANE Select	ENSP00000356379.4:n.9637-21A=
ENST00000680265.1:c.9859-21A=	ENSP00000505384.1:n.9859-21A=
ENST00000680710.1:c.9613-21A=	ENSP00000506676.1:n.9613-21A=
ENST00000294732.11:c.4882-21A=	ENSP00000294732.7:n.4882-21A=
ENST00000367408.5:c.2632-21A=	ENSP00000356378.1:n.2632-21A=
ENST00000367409.8:c.9637-21A=	ENSP00000356379.4:n.9637-21A=
ENST00000612785.1:c.3595-21A=	ENSP00000479244.1:n.3595-21A=
NM_001206846.1:c.4882-21A=	NP_001193775.1:n.4882-21A=
NM_018136.4:c.9637-21A=	NP_060606.3:n.9637-21A=
NM_018136.5:c.9637-21A= MANE Select	NP_060606.3:n.9637-21A=
NM_001206846.2:c.4882-21A=	NP_001193775.1:n.4882-21A=