Canonical Allele Identifier: CA1217925847

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090980T= , CM000663.2:g.197090980T=	GRCh38
NC_000001.10:g.197060110T= , CM000663.1:g.197060110T=	GRCh37
NC_000001.9:g.195326733T=	NCBI36
NG_015867.1:g.60715A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2793A=
ENST00000367409.9:c.9506A= MANE Select	ENSP00000356379.4:p.Lys3169=
ENST00000680265.1:c.9728A=	ENSP00000505384.1:p.Lys3243=
ENST00000680710.1:c.9482A=	ENSP00000506676.1:p.Lys3161=
ENST00000294732.11:c.4751A=	ENSP00000294732.7:p.Lys1584=
ENST00000367408.5:c.2501A=	ENSP00000356378.1:p.Lys834=
ENST00000367409.8:c.9506A=	ENSP00000356379.4:p.Lys3169=
ENST00000612785.1:c.3464A=	ENSP00000479244.1:p.Lys1155=
NM_001206846.1:c.4751A=	NP_001193775.1:p.Lys1584=
NM_018136.4:c.9506A=	NP_060606.3:p.Lys3169=
NM_018136.5:c.9506A= MANE Select	NP_060606.3:p.Lys3169=
NM_001206846.2:c.4751A=	NP_001193775.1:p.Lys1584=