Canonical Allele Identifier: CA343244302
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160100304T>A (hg19) chr1:g.160130514T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130514T>A , CM000663.2:g.160130514T>A GRCh38
NC_000001.10:g.160100304T>A , CM000663.1:g.160100304T>A GRCh37
NC_000001.9:g.158366928T>A NCBI36
NG_008014.1:g.19757T>A , LRG_6:g.19757T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1744T>A MANE Select ENSP00000354490.3:p.Phe582Ile
ENST00000361216.7:c.1744T>A ENSP00000354490.3:p.Phe582Ile
ENST00000392233.7:c.1744T>A ENSP00000376066.3:p.Phe582Ile
ENST00000447527.1:c.876T>A
ENST00000472488.5:n.1847T>A
NM_000702.3:c.1744T>A NP_000693.1:p.Phe582Ile
NM_000702.4:c.1744T>A MANE Select NP_000693.1:p.Phe582Ile
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