Canonical Allele Identifier: CA2336728027
Gene: ATP1A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41985092G= , CM000681.2:g.41985092G= GRCh38
NC_000019.9:g.42489244G= , CM000681.1:g.42489244G= GRCh37
NC_000019.8:g.47181084G= NCBI36
NG_008015.1:g.14139C=

Transcript Alleles

HGVS Amino-acid change
ENST00000545399.6:c.858C= ENSP00000444688.1:p.Pro286=
ENST00000644613.1:c.819C= ENSP00000494711.1:p.Pro273=
ENST00000648268.1:c.819C= MANE Select ENSP00000498113.1:p.Pro273=
ENST00000302102.9:c.819C= ENSP00000302397.5:p.Pro273=
ENST00000441343.5:c.819C= ENSP00000411503.1:p.Pro273=
ENST00000473086.3:c.729C= ENSP00000469129.2:p.Pro243=
ENST00000485672.2:n.132C=
ENST00000543770.5:c.852C= ENSP00000437577.1:p.Pro284=
ENST00000545399.5:c.858C= ENSP00000444688.1:p.Pro286=
ENST00000602133.5:c.729C= ENSP00000471581.1:p.Pro243=
NM_001256213.1:c.852C= NP_001243142.1:p.Pro284=
NM_001256214.1:c.858C= NP_001243143.1:p.Pro286=
NM_152296.4:c.819C= NP_689509.1:p.Pro273=
XM_011526991.1:c.729C= XP_011525293.1:p.Pro243=
NM_152296.5:c.819C= MANE Select NP_689509.1:p.Pro273=
NM_001256214.2:c.858C= NP_001243143.1:p.Pro286=
NM_001256213.2:c.852C= NP_001243142.1:p.Pro284=