Canonical Allele Identifier: CA2585369028
Gene: ATP1A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41970631_41970632insGT , CM000681.2:g.41970631_41970632insGT GRCh38
NC_000019.9:g.42474783_42474784insGT , CM000681.1:g.42474783_42474784insGT GRCh37
NC_000019.8:g.47166623_47166624insGT NCBI36
NG_008015.1:g.28600_28601insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000545399.6:c.2303-89_2303-88insCA ENSP00000444688.1:n.2303-89_2303-88insCA
ENST00000644613.1:c.2264-89_2264-88insCA ENSP00000494711.1:n.2264-89_2264-88insCA
ENST00000648268.1:c.2264-89_2264-88insCA MANE Select ENSP00000498113.1:n.2264-89_2264-88insCA
ENST00000302102.9:c.2264-89_2264-88insCA ENSP00000302397.5:n.2264-89_2264-88insCA
ENST00000441343.5:c.2264-89_2264-88insCA ENSP00000411503.1:n.2264-89_2264-88insCA
ENST00000543770.5:c.2297-89_2297-88insCA ENSP00000437577.1:n.2297-89_2297-88insCA
ENST00000545399.5:c.2303-89_2303-88insCA ENSP00000444688.1:n.2303-89_2303-88insCA
ENST00000602133.5:c.2174-89_2174-88insCA ENSP00000471581.1:n.2174-89_2174-88insCA
NM_001256213.1:c.2297-89_2297-88insCA NP_001243142.1:n.2297-89_2297-88insCA
NM_001256214.1:c.2303-89_2303-88insCA NP_001243143.1:n.2303-89_2303-88insCA
NM_152296.4:c.2264-89_2264-88insCA NP_689509.1:n.2264-89_2264-88insCA
XM_011526991.1:c.2174-89_2174-88insCA XP_011525293.1:n.2174-89_2174-88insCA
NM_152296.5:c.2264-89_2264-88insCA MANE Select NP_689509.1:n.2264-89_2264-88insCA
NM_001256214.2:c.2303-89_2303-88insCA NP_001243143.1:n.2303-89_2303-88insCA
NM_001256213.2:c.2297-89_2297-88insCA NP_001243142.1:n.2297-89_2297-88insCA