Canonical Allele Identifier: CA1217925164

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090245A= , CM000663.2:g.197090245A=	GRCh38
NC_000001.10:g.197059375A= , CM000663.1:g.197059375A=	GRCh37
NC_000001.9:g.195325998A=	NCBI36
NG_015867.1:g.61450T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3067T=
ENST00000367409.9:c.9780T= MANE Select	ENSP00000356379.4:p.Leu3260=
ENST00000680265.1:c.10002T=	ENSP00000505384.1:p.Leu3334=
ENST00000680710.1:c.9756T=	ENSP00000506676.1:p.Leu3252=
ENST00000294732.11:c.5025T=	ENSP00000294732.7:p.Leu1675=
ENST00000367408.5:c.2775T=	ENSP00000356378.1:p.Leu925=
ENST00000367409.8:c.9780T=	ENSP00000356379.4:p.Leu3260=
ENST00000612785.1:c.3738T=	ENSP00000479244.1:p.Leu1246=
NM_001206846.1:c.5025T=	NP_001193775.1:p.Leu1675=
NM_018136.4:c.9780T=	NP_060606.3:p.Leu3260=
NM_018136.5:c.9780T= MANE Select	NP_060606.3:p.Leu3260=
NM_001206846.2:c.5025T=	NP_001193775.1:p.Leu1675=