Canonical Allele Identifier: CA2336728111

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985268T= , CM000681.2:g.41985268T=	GRCh38
NC_000019.9:g.42489420T= , CM000681.1:g.42489420T=	GRCh37
NC_000019.8:g.47181260T=	NCBI36
NG_008015.1:g.13963A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.763+38A=	ENSP00000444688.1:n.763+38A=
ENST00000644613.1:c.724+38A=	ENSP00000494711.1:n.724+38A=
ENST00000645448.1:n.994A=
ENST00000648268.1:c.724+38A= MANE Select	ENSP00000498113.1:n.724+38A=
ENST00000302102.9:c.724+38A=	ENSP00000302397.5:n.724+38A=
ENST00000441343.5:c.724+38A=	ENSP00000411503.1:n.724+38A=
ENST00000473086.3:c.634+38A=	ENSP00000469129.2:n.634+38A=
ENST00000485672.2:n.37+38A=
ENST00000543770.5:c.757+38A=	ENSP00000437577.1:n.757+38A=
ENST00000545399.5:c.763+38A=	ENSP00000444688.1:n.763+38A=
ENST00000602133.5:c.634+38A=	ENSP00000471581.1:n.634+38A=
NM_001256213.1:c.757+38A=	NP_001243142.1:n.757+38A=
NM_001256214.1:c.763+38A=	NP_001243143.1:n.763+38A=
NM_152296.4:c.724+38A=	NP_689509.1:n.724+38A=
XM_011526991.1:c.634+38A=	XP_011525293.1:n.634+38A=
NM_152296.5:c.724+38A= MANE Select	NP_689509.1:n.724+38A=
NM_001256214.2:c.763+38A=	NP_001243143.1:n.763+38A=
NM_001256213.2:c.757+38A=	NP_001243142.1:n.757+38A=