Canonical Allele Identifier: CA2336728001

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985019_41985022delinsTGAA , CM000681.2:g.41985019_41985022delinsTGAA	GRCh38
NC_000019.9:g.42489171_42489174delinsTGAA , CM000681.1:g.42489171_42489174delinsTGAA	GRCh37
NC_000019.8:g.47181011_47181014delinsTGAA	NCBI36
NG_008015.1:g.14209_14212delinsTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.928_931delinsTTCA	ENSP00000444688.1:p.Phe310=
ENST00000644613.1:c.889_892delinsTTCA	ENSP00000494711.1:p.Phe297=
ENST00000648268.1:c.889_892delinsTTCA MANE Select	ENSP00000498113.1:p.Phe297=
ENST00000302102.9:c.889_892delinsTTCA	ENSP00000302397.5:p.Phe297=
ENST00000441343.5:c.889_892delinsTTCA	ENSP00000411503.1:p.Phe297=
ENST00000485672.2:n.202_205delinsTTCA
ENST00000543770.5:c.922_925delinsTTCA	ENSP00000437577.1:p.Phe308=
ENST00000545399.5:c.928_931delinsTTCA	ENSP00000444688.1:p.Phe310=
ENST00000602133.5:c.799_802delinsTTCA	ENSP00000471581.1:p.Phe267=
NM_001256213.1:c.922_925delinsTTCA	NP_001243142.1:p.Phe308=
NM_001256214.1:c.928_931delinsTTCA	NP_001243143.1:p.Phe310=
NM_152296.4:c.889_892delinsTTCA	NP_689509.1:p.Phe297=
XM_011526991.1:c.799_802delinsTTCA	XP_011525293.1:p.Phe267=
NM_152296.5:c.889_892delinsTTCA MANE Select	NP_689509.1:p.Phe297=
NM_001256214.2:c.928_931delinsTTCA	NP_001243143.1:p.Phe310=
NM_001256213.2:c.922_925delinsTTCA	NP_001243142.1:p.Phe308=