Canonical Allele Identifier: CA2336728057

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985178_41985179delinsGA , CM000681.2:g.41985178_41985179delinsGA	GRCh38
NC_000019.9:g.42489330_42489331delinsGA , CM000681.1:g.42489330_42489331delinsGA	GRCh37
NC_000019.8:g.47181170_47181171delinsGA	NCBI36
NG_008015.1:g.14052_14053delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.771_772delinsTC	ENSP00000444688.1:p.Ala257=
ENST00000644613.1:c.732_733delinsTC	ENSP00000494711.1:p.Ala244=
ENST00000648268.1:c.732_733delinsTC MANE Select	ENSP00000498113.1:p.Ala244=
ENST00000302102.9:c.732_733delinsTC	ENSP00000302397.5:p.Ala244=
ENST00000441343.5:c.732_733delinsTC	ENSP00000411503.1:p.Ala244=
ENST00000473086.3:c.642_643delinsTC	ENSP00000469129.2:p.Ala214=
ENST00000485672.2:n.45_46delinsTC
ENST00000543770.5:c.765_766delinsTC	ENSP00000437577.1:p.Ala255=
ENST00000545399.5:c.771_772delinsTC	ENSP00000444688.1:p.Ala257=
ENST00000602133.5:c.642_643delinsTC	ENSP00000471581.1:p.Ala214=
NM_001256213.1:c.765_766delinsTC	NP_001243142.1:p.Ala255=
NM_001256214.1:c.771_772delinsTC	NP_001243143.1:p.Ala257=
NM_152296.4:c.732_733delinsTC	NP_689509.1:p.Ala244=
XM_011526991.1:c.642_643delinsTC	XP_011525293.1:p.Ala214=
NM_152296.5:c.732_733delinsTC MANE Select	NP_689509.1:p.Ala244=
NM_001256214.2:c.771_772delinsTC	NP_001243143.1:p.Ala257=
NM_001256213.2:c.765_766delinsTC	NP_001243142.1:p.Ala255=