Canonical Allele Identifier: CA2336728026
Gene: ATP1A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41985091T= , CM000681.2:g.41985091T= GRCh38
NC_000019.9:g.42489243T= , CM000681.1:g.42489243T= GRCh37
NC_000019.8:g.47181083T= NCBI36
NG_008015.1:g.14140A=

Transcript Alleles

HGVS Amino-acid change
ENST00000545399.6:c.859A= ENSP00000444688.1:p.Ile287=
ENST00000644613.1:c.820A= ENSP00000494711.1:p.Ile274=
ENST00000648268.1:c.820A= MANE Select ENSP00000498113.1:p.Ile274=
ENST00000302102.9:c.820A= ENSP00000302397.5:p.Ile274=
ENST00000441343.5:c.820A= ENSP00000411503.1:p.Ile274=
ENST00000473086.3:c.730A= ENSP00000469129.2:p.Ile244=
ENST00000485672.2:n.133A=
ENST00000543770.5:c.853A= ENSP00000437577.1:p.Ile285=
ENST00000545399.5:c.859A= ENSP00000444688.1:p.Ile287=
ENST00000602133.5:c.730A= ENSP00000471581.1:p.Ile244=
NM_001256213.1:c.853A= NP_001243142.1:p.Ile285=
NM_001256214.1:c.859A= NP_001243143.1:p.Ile287=
NM_152296.4:c.820A= NP_689509.1:p.Ile274=
XM_011526991.1:c.730A= XP_011525293.1:p.Ile244=
NM_152296.5:c.820A= MANE Select NP_689509.1:p.Ile274=
NM_001256214.2:c.859A= NP_001243143.1:p.Ile287=
NM_001256213.2:c.853A= NP_001243142.1:p.Ile285=