Canonical Allele Identifier: CA2336728145

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985364A= , CM000681.2:g.41985364A=	GRCh38
NC_000019.9:g.42489516A= , CM000681.1:g.42489516A=	GRCh37
NC_000019.8:g.47181356A=	NCBI36
NG_008015.1:g.13867T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.705T=	ENSP00000444688.1:p.Thr235=
ENST00000644613.1:c.666T=	ENSP00000494711.1:p.Thr222=
ENST00000645448.1:n.898T=
ENST00000648268.1:c.666T= MANE Select	ENSP00000498113.1:p.Thr222=
ENST00000302102.9:c.666T=	ENSP00000302397.5:p.Thr222=
ENST00000441343.5:c.666T=	ENSP00000411503.1:p.Thr222=
ENST00000473086.3:c.576T=	ENSP00000469129.2:p.Thr192=
ENST00000543770.5:c.699T=	ENSP00000437577.1:p.Thr233=
ENST00000545399.5:c.705T=	ENSP00000444688.1:p.Thr235=
ENST00000602133.5:c.576T=	ENSP00000471581.1:p.Thr192=
NM_001256213.1:c.699T=	NP_001243142.1:p.Thr233=
NM_001256214.1:c.705T=	NP_001243143.1:p.Thr235=
NM_152296.4:c.666T=	NP_689509.1:p.Thr222=
XM_011526991.1:c.576T=	XP_011525293.1:p.Thr192=
NM_152296.5:c.666T= MANE Select	NP_689509.1:p.Thr222=
NM_001256214.2:c.705T=	NP_001243143.1:p.Thr235=
NM_001256213.2:c.699T=	NP_001243142.1:p.Thr233=