Canonical Allele Identifier: CA421599585

Gene: ATP1A2

Linked Data

• MyVariant Identifiers: chr1:g.160097418G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127628G>T , CM000663.2:g.160127628G>T	GRCh38
NC_000001.10:g.160097418G>T , CM000663.1:g.160097418G>T	GRCh37
NC_000001.9:g.158364042G>T	NCBI36
NG_008014.1:g.16871G>T , LRG_6:g.16871G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.825G>T MANE Select	ENSP00000354490.3:p.Leu275=
ENST00000361216.7:c.825G>T	ENSP00000354490.3:p.Leu275=
ENST00000392233.7:c.825G>T	ENSP00000376066.3:p.Leu275=
ENST00000472488.5:n.928G>T
NM_000702.3:c.825G>T	NP_000693.1:p.Leu275=
NM_000702.4:c.825G>T MANE Select	NP_000693.1:p.Leu275=