Canonical Allele Identifier: CA1217925122

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090197T= , CM000663.2:g.197090197T=	GRCh38
NC_000001.10:g.197059327T= , CM000663.1:g.197059327T=	GRCh37
NC_000001.9:g.195325950T=	NCBI36
NG_015867.1:g.61498A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3115A=
ENST00000367409.9:c.9828A= MANE Select	ENSP00000356379.4:p.Leu3276=
ENST00000680265.1:c.10050A=	ENSP00000505384.1:p.Leu3350=
ENST00000680710.1:c.9804A=	ENSP00000506676.1:p.Leu3268=
ENST00000294732.11:c.5073A=	ENSP00000294732.7:p.Leu1691=
ENST00000367408.5:c.2823A=	ENSP00000356378.1:p.Leu941=
ENST00000367409.8:c.9828A=	ENSP00000356379.4:p.Leu3276=
ENST00000612785.1:c.3786A=	ENSP00000479244.1:p.Leu1262=
NM_001206846.1:c.5073A=	NP_001193775.1:p.Leu1691=
NM_018136.4:c.9828A=	NP_060606.3:p.Leu3276=
NM_018136.5:c.9828A= MANE Select	NP_060606.3:p.Leu3276=
NM_001206846.2:c.5073A=	NP_001193775.1:p.Leu1691=