Canonical Allele Identifier: CA1143037804

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197121834G= , CM000663.2:g.197121834G=	GRCh38
NC_000001.10:g.197090964G= , CM000663.1:g.197090964G=	GRCh37
NC_000001.9:g.195357587G=	NCBI36
NG_015867.1:g.29861C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1912+81C=
ENST00000367409.9:c.3870+81C= MANE Select	ENSP00000356379.4:n.3870+81C=
ENST00000680265.1:c.3870+81C=	ENSP00000505384.1:n.3870+81C=
ENST00000680710.1:c.3870+81C=	ENSP00000506676.1:n.3870+81C=
ENST00000681879.1:c.3918+33C=	ENSP00000505363.1:n.3918+33C=
ENST00000294732.11:c.3870+81C=	ENSP00000294732.7:n.3870+81C=
ENST00000367408.5:c.1620+81C=	ENSP00000356378.1:n.1620+81C=
ENST00000367409.8:c.3870+81C=	ENSP00000356379.4:n.3870+81C=
ENST00000612785.1:c.562-19187C=	ENSP00000479244.1:n.562-19187C=
NM_001206846.1:c.3870+81C=	NP_001193775.1:n.3870+81C=
NM_018136.4:c.3870+81C=	NP_060606.3:n.3870+81C=
NM_018136.5:c.3870+81C= MANE Select	NP_060606.3:n.3870+81C=
NM_001206846.2:c.3870+81C=	NP_001193775.1:n.3870+81C=