Canonical Allele Identifier: CA2336724902

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41978193G= , CM000681.2:g.41978193G=	GRCh38
NC_000019.9:g.42482345G= , CM000681.1:g.42482345G=	GRCh37
NC_000019.8:g.47174185G=	NCBI36
NG_008015.1:g.21038C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.1803C=	ENSP00000444688.1:p.Ala601=
ENST00000644613.1:c.1764C=	ENSP00000494711.1:p.Ala588=
ENST00000648268.1:c.1764C= MANE Select	ENSP00000498113.1:p.Ala588=
ENST00000302102.9:c.1764C=	ENSP00000302397.5:p.Ala588=
ENST00000441343.5:c.1764C=	ENSP00000411503.1:p.Ala588=
ENST00000543770.5:c.1797C=	ENSP00000437577.1:p.Ala599=
ENST00000545399.5:c.1803C=	ENSP00000444688.1:p.Ala601=
ENST00000602133.5:c.1674C=	ENSP00000471581.1:p.Ala558=
NM_001256213.1:c.1797C=	NP_001243142.1:p.Ala599=
NM_001256214.1:c.1803C=	NP_001243143.1:p.Ala601=
NM_152296.4:c.1764C=	NP_689509.1:p.Ala588=
XM_011526991.1:c.1674C=	XP_011525293.1:p.Ala558=
NM_152296.5:c.1764C= MANE Select	NP_689509.1:p.Ala588=
NM_001256214.2:c.1803C=	NP_001243143.1:p.Ala601=
NM_001256213.2:c.1797C=	NP_001243142.1:p.Ala599=