Canonical Allele Identifier: CA1143210877

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088376C= , CM000663.2:g.197088376C=	GRCh38
NC_000001.10:g.197057506C= , CM000663.1:g.197057506C=	GRCh37
NC_000001.9:g.195324129C=	NCBI36
NG_015867.1:g.63319G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3328G=
ENST00000367409.9:c.10041G= MANE Select	ENSP00000356379.4:p.Leu3347=
ENST00000680265.1:c.10263G=	ENSP00000505384.1:p.Leu3421=
ENST00000680710.1:c.10017G=	ENSP00000506676.1:p.Leu3339=
ENST00000294732.11:c.5286G=	ENSP00000294732.7:p.Leu1762=
ENST00000367408.5:c.3036G=	ENSP00000356378.1:p.Leu1012=
ENST00000367409.8:c.10041G=	ENSP00000356379.4:p.Leu3347=
ENST00000612785.1:c.3999G=	ENSP00000479244.1:p.Leu1333=
NM_001206846.1:c.5286G=	NP_001193775.1:p.Leu1762=
NM_018136.4:c.10041G=	NP_060606.3:p.Leu3347=
NM_018136.5:c.10041G= MANE Select	NP_060606.3:p.Leu3347=
NM_001206846.2:c.5286G=	NP_001193775.1:p.Leu1762=