Canonical Allele Identifier: CA421599343

Gene: ATP1A2

Linked Data

• MyVariant Identifiers: chr1:g.160097343C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127553C>G , CM000663.2:g.160127553C>G	GRCh38
NC_000001.10:g.160097343C>G , CM000663.1:g.160097343C>G	GRCh37
NC_000001.9:g.158363967C>G	NCBI36
NG_008014.1:g.16796C>G , LRG_6:g.16796C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.750C>G MANE Select	ENSP00000354490.3:p.Gly250=
ENST00000361216.7:c.750C>G	ENSP00000354490.3:p.Gly250=
ENST00000392233.7:c.750C>G	ENSP00000376066.3:p.Gly250=
ENST00000472488.5:n.853C>G
NM_000702.3:c.750C>G	NP_000693.1:p.Gly250=
NM_000702.4:c.750C>G MANE Select	NP_000693.1:p.Gly250=