Canonical Allele Identifier: CA1217926682

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093099T= , CM000663.2:g.197093099T=	GRCh38
NC_000001.10:g.197062229T= , CM000663.1:g.197062229T=	GRCh37
NC_000001.9:g.195328852T=	NCBI36
NG_015867.1:g.58596A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2534A=
ENST00000367409.9:c.9247A= MANE Select	ENSP00000356379.4:p.Thr3083=
ENST00000680265.1:c.9469A=	ENSP00000505384.1:p.Thr3157=
ENST00000680710.1:c.9247A=	ENSP00000506676.1:p.Thr3083=
ENST00000294732.11:c.4492A=	ENSP00000294732.7:p.Thr1498=
ENST00000367408.5:c.2242A=	ENSP00000356378.1:p.Thr748=
ENST00000367409.8:c.9247A=	ENSP00000356379.4:p.Thr3083=
ENST00000612785.1:c.3205A=	ENSP00000479244.1:p.Thr1069=
NM_001206846.1:c.4492A=	NP_001193775.1:p.Thr1498=
NM_018136.4:c.9247A=	NP_060606.3:p.Thr3083=
NM_018136.5:c.9247A= MANE Select	NP_060606.3:p.Thr3083=
NM_001206846.2:c.4492A=	NP_001193775.1:p.Thr1498=