Canonical Allele Identifier: CA2585370621
Gene: ATP1A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41984850T>A , CM000681.2:g.41984850T>A GRCh38
NC_000019.9:g.42489002T>A , CM000681.1:g.42489002T>A GRCh37
NC_000019.8:g.47180842T>A NCBI36
NG_008015.1:g.14381A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000545399.6:c.1032+68A>T ENSP00000444688.1:n.1032+68A>T
ENST00000644613.1:c.993+68A>T ENSP00000494711.1:n.993+68A>T
ENST00000648268.1:c.993+68A>T MANE Select ENSP00000498113.1:n.993+68A>T
ENST00000302102.9:c.993+68A>T ENSP00000302397.5:n.993+68A>T
ENST00000441343.5:c.993+68A>T ENSP00000411503.1:n.993+68A>T
ENST00000485672.2:n.374A>T
ENST00000543770.5:c.1026+68A>T ENSP00000437577.1:n.1026+68A>T
ENST00000545399.5:c.1032+68A>T ENSP00000444688.1:n.1032+68A>T
ENST00000602133.5:c.903+68A>T ENSP00000471581.1:n.903+68A>T
NM_001256213.1:c.1026+68A>T NP_001243142.1:n.1026+68A>T
NM_001256214.1:c.1032+68A>T NP_001243143.1:n.1032+68A>T
NM_152296.4:c.993+68A>T NP_689509.1:n.993+68A>T
XM_011526991.1:c.903+68A>T XP_011525293.1:n.903+68A>T
NM_152296.5:c.993+68A>T MANE Select NP_689509.1:n.993+68A>T
NM_001256214.2:c.1032+68A>T NP_001243143.1:n.1032+68A>T
NM_001256213.2:c.1026+68A>T NP_001243142.1:n.1026+68A>T