Canonical Allele Identifier: CA1202191862
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127637_160127638delinsGC , CM000663.2:g.160127637_160127638delinsGC GRCh38
NC_000001.10:g.160097427_160097428delinsGC , CM000663.1:g.160097427_160097428delinsGC GRCh37
NC_000001.9:g.158364051_158364052delinsGC NCBI36
NG_008014.1:g.16880_16881delinsGC , LRG_6:g.16880_16881delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.834_835delinsGC MANE Select ENSP00000354490.3:p.Gly278=
ENST00000361216.7:c.834_835delinsGC ENSP00000354490.3:p.Gly278=
ENST00000392233.7:c.834_835delinsGC ENSP00000376066.3:p.Gly278=
ENST00000472488.5:n.937_938delinsGC
NM_000702.3:c.834_835delinsGC NP_000693.1:p.Gly278=
NM_000702.4:c.834_835delinsGC MANE Select NP_000693.1:p.Gly278=
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