Canonical Allele Identifier: CA1217926680

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093089A= , CM000663.2:g.197093089A=	GRCh38
NC_000001.10:g.197062219A= , CM000663.1:g.197062219A=	GRCh37
NC_000001.9:g.195328842A=	NCBI36
NG_015867.1:g.58606T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2544T=
ENST00000367409.9:c.9257T= MANE Select	ENSP00000356379.4:p.Leu3086=
ENST00000680265.1:c.9479T=	ENSP00000505384.1:p.Leu3160=
ENST00000680710.1:c.9257T=	ENSP00000506676.1:p.Leu3086=
ENST00000294732.11:c.4502T=	ENSP00000294732.7:p.Leu1501=
ENST00000367408.5:c.2252T=	ENSP00000356378.1:p.Leu751=
ENST00000367409.8:c.9257T=	ENSP00000356379.4:p.Leu3086=
ENST00000612785.1:c.3215T=	ENSP00000479244.1:p.Leu1072=
NM_001206846.1:c.4502T=	NP_001193775.1:p.Leu1501=
NM_018136.4:c.9257T=	NP_060606.3:p.Leu3086=
NM_018136.5:c.9257T= MANE Select	NP_060606.3:p.Leu3086=
NM_001206846.2:c.4502T=	NP_001193775.1:p.Leu1501=