Canonical Allele Identifier: CA343237719

Gene: ATP1A2

Linked Data

• MyVariant Identifiers: chr1:g.160097453A>T (hg19) ; chr1:g.160127663A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127663A>T , CM000663.2:g.160127663A>T	GRCh38
NC_000001.10:g.160097453A>T , CM000663.1:g.160097453A>T	GRCh37
NC_000001.9:g.158364077A>T	NCBI36
NG_008014.1:g.16906A>T , LRG_6:g.16906A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.860A>T MANE Select	ENSP00000354490.3:p.Glu287Val
ENST00000361216.7:c.860A>T	ENSP00000354490.3:p.Glu287Val
ENST00000392233.7:c.860A>T	ENSP00000376066.3:p.Glu287Val
ENST00000472488.5:n.963A>T
NM_000702.3:c.860A>T	NP_000693.1:p.Glu287Val
NM_000702.4:c.860A>T MANE Select	NP_000693.1:p.Glu287Val