Canonical Allele Identifier: CA2336727979
Gene: ATP1A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41984944G= , CM000681.2:g.41984944G= GRCh38
NC_000019.9:g.42489096G= , CM000681.1:g.42489096G= GRCh37
NC_000019.8:g.47180936G= NCBI36
NG_008015.1:g.14287C=

Transcript Alleles

HGVS Amino-acid change
ENST00000545399.6:c.1006C= ENSP00000444688.1:p.Pro336=
ENST00000644613.1:c.967C= ENSP00000494711.1:p.Pro323=
ENST00000648268.1:c.967C= MANE Select ENSP00000498113.1:p.Pro323=
ENST00000302102.9:c.967C= ENSP00000302397.5:p.Pro323=
ENST00000441343.5:c.967C= ENSP00000411503.1:p.Pro323=
ENST00000485672.2:n.280C=
ENST00000543770.5:c.1000C= ENSP00000437577.1:p.Pro334=
ENST00000545399.5:c.1006C= ENSP00000444688.1:p.Pro336=
ENST00000602133.5:c.877C= ENSP00000471581.1:p.Pro293=
NM_001256213.1:c.1000C= NP_001243142.1:p.Pro334=
NM_001256214.1:c.1006C= NP_001243143.1:p.Pro336=
NM_152296.4:c.967C= NP_689509.1:p.Pro323=
XM_011526991.1:c.877C= XP_011525293.1:p.Pro293=
NM_152296.5:c.967C= MANE Select NP_689509.1:p.Pro323=
NM_001256214.2:c.1006C= NP_001243143.1:p.Pro336=
NM_001256213.2:c.1000C= NP_001243142.1:p.Pro334=