Canonical Allele Identifier: CA422672226

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057527T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088397T>C , CM000663.2:g.197088397T>C	GRCh38
NC_000001.10:g.197057527T>C , CM000663.1:g.197057527T>C	GRCh37
NC_000001.9:g.195324150T>C	NCBI36
NG_015867.1:g.63298A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3307A>G
ENST00000367409.9:c.10020A>G MANE Select	ENSP00000356379.4:p.Glu3340=
ENST00000680265.1:c.10242A>G	ENSP00000505384.1:p.Glu3414=
ENST00000680710.1:c.9996A>G	ENSP00000506676.1:p.Glu3332=
ENST00000294732.11:c.5265A>G	ENSP00000294732.7:p.Glu1755=
ENST00000367408.5:c.3015A>G	ENSP00000356378.1:p.Glu1005=
ENST00000367409.8:c.10020A>G	ENSP00000356379.4:p.Glu3340=
ENST00000612785.1:c.3978A>G	ENSP00000479244.1:p.Glu1326=
NM_001206846.1:c.5265A>G	NP_001193775.1:p.Glu1755=
NM_018136.4:c.10020A>G	NP_060606.3:p.Glu3340=
NM_018136.5:c.10020A>G MANE Select	NP_060606.3:p.Glu3340=
NM_001206846.2:c.5265A>G	NP_001193775.1:p.Glu1755=