Canonical Allele Identifier: CA1217926684

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093102A= , CM000663.2:g.197093102A=	GRCh38
NC_000001.10:g.197062232A= , CM000663.1:g.197062232A=	GRCh37
NC_000001.9:g.195328855A=	NCBI36
NG_015867.1:g.58593T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2531T=
ENST00000367409.9:c.9244T= MANE Select	ENSP00000356379.4:p.Ser3082=
ENST00000680265.1:c.9466T=	ENSP00000505384.1:p.Ser3156=
ENST00000680710.1:c.9244T=	ENSP00000506676.1:p.Ser3082=
ENST00000294732.11:c.4489T=	ENSP00000294732.7:p.Ser1497=
ENST00000367408.5:c.2239T=	ENSP00000356378.1:p.Ser747=
ENST00000367409.8:c.9244T=	ENSP00000356379.4:p.Ser3082=
ENST00000612785.1:c.3202T=	ENSP00000479244.1:p.Ser1068=
NM_001206846.1:c.4489T=	NP_001193775.1:p.Ser1497=
NM_018136.4:c.9244T=	NP_060606.3:p.Ser3082=
NM_018136.5:c.9244T= MANE Select	NP_060606.3:p.Ser3082=
NM_001206846.2:c.4489T=	NP_001193775.1:p.Ser1497=