Canonical Allele Identifier: CA2840693854
Gene: ATP1A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41970342dup , CM000681.2:g.41970342dup GRCh38
NC_000019.9:g.42474494dup , CM000681.1:g.42474494dup GRCh37
NC_000019.8:g.47166334dup NCBI36
NG_008015.1:g.28892dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000545399.6:c.2458-31dup ENSP00000444688.1:n.2458-31dup
ENST00000644613.1:c.2419-31dup ENSP00000494711.1:n.2419-31dup
ENST00000648268.1:c.2419-31dup MANE Select ENSP00000498113.1:n.2419-31dup
ENST00000302102.9:c.2419-31dup ENSP00000302397.5:n.2419-31dup
ENST00000441343.5:c.2419-31dup ENSP00000411503.1:n.2419-31dup
ENST00000543770.5:c.2452-31dup ENSP00000437577.1:n.2452-31dup
ENST00000545399.5:c.2458-31dup ENSP00000444688.1:n.2458-31dup
ENST00000602133.5:c.2329-31dup ENSP00000471581.1:n.2329-31dup
NM_001256213.1:c.2452-31dup NP_001243142.1:n.2452-31dup
NM_001256214.1:c.2458-31dup NP_001243143.1:n.2458-31dup
NM_152296.4:c.2419-31dup NP_689509.1:n.2419-31dup
XM_011526991.1:c.2329-31dup XP_011525293.1:n.2329-31dup
NM_152296.5:c.2419-31dup MANE Select NP_689509.1:n.2419-31dup
NM_001256214.2:c.2458-31dup NP_001243143.1:n.2458-31dup
NM_001256213.2:c.2452-31dup NP_001243142.1:n.2452-31dup