Canonical Allele Identifier: CA2839646079

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41982195del , CM000681.2:g.41982195del	GRCh38
NC_000019.9:g.42486347del , CM000681.1:g.42486347del	GRCh37
NC_000019.8:g.47178187del	NCBI36
NG_008015.1:g.17038del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.1033-87del	ENSP00000444688.1:n.1033-87del
ENST00000644613.1:c.994-87del	ENSP00000494711.1:n.994-87del
ENST00000648268.1:c.994-87del MANE Select	ENSP00000498113.1:n.994-87del
ENST00000302102.9:c.994-87del	ENSP00000302397.5:n.994-87del
ENST00000441343.5:c.994-87del	ENSP00000411503.1:n.994-87del
ENST00000543770.5:c.1027-87del	ENSP00000437577.1:n.1027-87del
ENST00000545399.5:c.1033-87del	ENSP00000444688.1:n.1033-87del
ENST00000602133.5:c.904-87del	ENSP00000471581.1:n.904-87del
NM_001256213.1:c.1027-87del	NP_001243142.1:n.1027-87del
NM_001256214.1:c.1033-87del	NP_001243143.1:n.1033-87del
NM_152296.4:c.994-87del	NP_689509.1:n.994-87del
XM_011526991.1:c.904-87del	XP_011525293.1:n.904-87del
NM_152296.5:c.994-87del MANE Select	NP_689509.1:n.994-87del
NM_001256214.2:c.1033-87del	NP_001243143.1:n.1033-87del
NM_001256213.2:c.1027-87del	NP_001243142.1:n.1027-87del