Canonical Allele Identifier: CA422672331

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059462A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090332A>T , CM000663.2:g.197090332A>T	GRCh38
NC_000001.10:g.197059462A>T , CM000663.1:g.197059462A>T	GRCh37
NC_000001.9:g.195326085A>T	NCBI36
NG_015867.1:g.61363T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2980T>A
ENST00000367409.9:c.9693T>A MANE Select	ENSP00000356379.4:p.Ala3231=
ENST00000680265.1:c.9915T>A	ENSP00000505384.1:p.Ala3305=
ENST00000680710.1:c.9669T>A	ENSP00000506676.1:p.Ala3223=
ENST00000294732.11:c.4938T>A	ENSP00000294732.7:p.Ala1646=
ENST00000367408.5:c.2688T>A	ENSP00000356378.1:p.Ala896=
ENST00000367409.8:c.9693T>A	ENSP00000356379.4:p.Ala3231=
ENST00000612785.1:c.3651T>A	ENSP00000479244.1:p.Ala1217=
NM_001206846.1:c.4938T>A	NP_001193775.1:p.Ala1646=
NM_018136.4:c.9693T>A	NP_060606.3:p.Ala3231=
NM_018136.5:c.9693T>A MANE Select	NP_060606.3:p.Ala3231=
NM_001206846.2:c.4938T>A	NP_001193775.1:p.Ala1646=