Canonical Allele Identifier: CA1217925853

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090992T= , CM000663.2:g.197090992T=	GRCh38
NC_000001.10:g.197060122T= , CM000663.1:g.197060122T=	GRCh37
NC_000001.9:g.195326745T=	NCBI36
NG_015867.1:g.60703A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2781A=
ENST00000367409.9:c.9494A= MANE Select	ENSP00000356379.4:p.His3165=
ENST00000680265.1:c.9716A=	ENSP00000505384.1:p.His3239=
ENST00000680710.1:c.9470A=	ENSP00000506676.1:p.His3157=
ENST00000294732.11:c.4739A=	ENSP00000294732.7:p.His1580=
ENST00000367408.5:c.2489A=	ENSP00000356378.1:p.His830=
ENST00000367409.8:c.9494A=	ENSP00000356379.4:p.His3165=
ENST00000612785.1:c.3452A=	ENSP00000479244.1:p.His1151=
NM_001206846.1:c.4739A=	NP_001193775.1:p.His1580=
NM_018136.4:c.9494A=	NP_060606.3:p.His3165=
NM_018136.5:c.9494A= MANE Select	NP_060606.3:p.His3165=
NM_001206846.2:c.4739A=	NP_001193775.1:p.His1580=