Canonical Allele Identifier: CA406045921
Gene: ATP1A3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41978276A>C , CM000681.2:g.41978276A>C GRCh38
NC_000019.9:g.42482428A>C , CM000681.1:g.42482428A>C GRCh37
NC_000019.8:g.47174268A>C NCBI36
NG_008015.1:g.20955T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000545399.6:c.1720T>G ENSP00000444688.1:p.Phe574Val
ENST00000644613.1:c.1681T>G ENSP00000494711.1:p.Phe561Val
ENST00000648268.1:c.1681T>G MANE Select ENSP00000498113.1:p.Phe561Val
ENST00000302102.9:c.1681T>G ENSP00000302397.5:p.Phe561Val
ENST00000441343.5:c.1681T>G ENSP00000411503.1:p.Phe561Val
ENST00000543770.5:c.1714T>G ENSP00000437577.1:p.Phe572Val
ENST00000545399.5:c.1720T>G ENSP00000444688.1:p.Phe574Val
ENST00000602133.5:c.1591T>G ENSP00000471581.1:p.Phe531Val
NM_001256213.1:c.1714T>G NP_001243142.1:p.Phe572Val
NM_001256214.1:c.1720T>G NP_001243143.1:p.Phe574Val
NM_152296.4:c.1681T>G NP_689509.1:p.Phe561Val
XM_011526991.1:c.1591T>G XP_011525293.1:p.Phe531Val
NM_152296.5:c.1681T>G MANE Select NP_689509.1:p.Phe561Val
NM_001256214.2:c.1720T>G NP_001243143.1:p.Phe574Val
NM_001256213.2:c.1714T>G NP_001243142.1:p.Phe572Val