Canonical Allele Identifier: CA2536253556
Gene: ATP1A3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41984913_41984914insCAGCCCTCACC , CM000681.2:g.41984913_41984914insCAGCCCTCACC GRCh38
NC_000019.9:g.42489065_42489066insCAGCCCTCACC , CM000681.1:g.42489065_42489066insCAGCCCTCACC GRCh37
NC_000019.8:g.47180905_47180906insCAGCCCTCACC NCBI36
NG_008015.1:g.14319_14320insTGAGGGCTGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000545399.6:c.1032+6_1032+7insTGAGGGCTGGG ENSP00000444688.1:n.1032+6_1032+7insTGAGGGCTGGG
ENST00000644613.1:c.993+6_993+7insTGAGGGCTGGG ENSP00000494711.1:n.993+6_993+7insTGAGGGCTGGG
ENST00000648268.1:c.993+6_993+7insTGAGGGCTGGG MANE Select ENSP00000498113.1:n.993+6_993+7insTGAGGGCTGGG
ENST00000302102.9:c.993+6_993+7insTGAGGGCTGGG ENSP00000302397.5:n.993+6_993+7insTGAGGGCTGGG
ENST00000441343.5:c.993+6_993+7insTGAGGGCTGGG ENSP00000411503.1:n.993+6_993+7insTGAGGGCTGGG
ENST00000485672.2:n.312_313insTGAGGGCTGGG
ENST00000543770.5:c.1026+6_1026+7insTGAGGGCTGGG ENSP00000437577.1:n.1026+6_1026+7insTGAGGGCTGGG
ENST00000545399.5:c.1032+6_1032+7insTGAGGGCTGGG ENSP00000444688.1:n.1032+6_1032+7insTGAGGGCTGGG
ENST00000602133.5:c.903+6_903+7insTGAGGGCTGGG ENSP00000471581.1:n.903+6_903+7insTGAGGGCTGGG
NM_001256213.1:c.1026+6_1026+7insTGAGGGCTGGG NP_001243142.1:n.1026+6_1026+7insTGAGGGCTGGG
NM_001256214.1:c.1032+6_1032+7insTGAGGGCTGGG NP_001243143.1:n.1032+6_1032+7insTGAGGGCTGGG
NM_152296.4:c.993+6_993+7insTGAGGGCTGGG NP_689509.1:n.993+6_993+7insTGAGGGCTGGG
XM_011526991.1:c.903+6_903+7insTGAGGGCTGGG XP_011525293.1:n.903+6_903+7insTGAGGGCTGGG
NM_152296.5:c.993+6_993+7insTGAGGGCTGGG MANE Select NP_689509.1:n.993+6_993+7insTGAGGGCTGGG
NM_001256214.2:c.1032+6_1032+7insTGAGGGCTGGG NP_001243143.1:n.1032+6_1032+7insTGAGGGCTGGG
NM_001256213.2:c.1026+6_1026+7insTGAGGGCTGGG NP_001243142.1:n.1026+6_1026+7insTGAGGGCTGGG