Canonical Allele Identifier: CA526594039

Gene: ATP1A2

Linked Data

• dbSNP Id: rs1558010403
• gnomAD v2: 1-160109810-G-A
• gnomAD v4: 1-160140020-G-A
• MyVariant Identifiers: chr1:g.160109810G>A (hg19) ; chr1:g.160140020G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160140020G>A , CM000663.2:g.160140020G>A	GRCh38
NC_000001.10:g.160109810G>A , CM000663.1:g.160109810G>A	GRCh37
NC_000001.9:g.158376434G>A	NCBI36
NG_008014.1:g.29263G>A , LRG_6:g.29263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.3034+36G>A MANE Select	ENSP00000354490.3:n.3034+36G>A
ENST00000361216.7:c.3034+36G>A	ENSP00000354490.3:n.3034+36G>A
ENST00000392233.7:c.3001+36G>A	ENSP00000376066.3:n.3001+36G>A
ENST00000447527.1:c.2115+36G>A
ENST00000459972.1:n.26+36G>A
ENST00000463989.1:n.406G>A
NM_000702.3:c.3034+36G>A	NP_000693.1:n.3034+36G>A
NM_000702.4:c.3034+36G>A MANE Select	NP_000693.1:n.3034+36G>A