Canonical Allele Identifier: CA920112506

Gene: ATP1A3

Linked Data

• dbSNP Id: rs1599722242

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41984786delinsAC , CM000681.2:g.41984786delinsAC	GRCh38
NC_000019.9:g.42488938delinsAC , CM000681.1:g.42488938delinsAC	GRCh37
NC_000019.8:g.47180778delinsAC	NCBI36
NG_008015.1:g.14445delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.1032+132delinsGT	ENSP00000444688.1:n.1032+132delinsGT
ENST00000644613.1:c.993+132delinsGT	ENSP00000494711.1:n.993+132delinsGT
ENST00000648268.1:c.993+132delinsGT MANE Select	ENSP00000498113.1:n.993+132delinsGT
ENST00000302102.9:c.993+132delinsGT	ENSP00000302397.5:n.993+132delinsGT
ENST00000441343.5:c.993+132delinsGT	ENSP00000411503.1:n.993+132delinsGT
ENST00000485672.2:n.438delinsGT
ENST00000543770.5:c.1026+132delinsGT	ENSP00000437577.1:n.1026+132delinsGT
ENST00000545399.5:c.1032+132delinsGT	ENSP00000444688.1:n.1032+132delinsGT
ENST00000602133.5:c.903+132delinsGT	ENSP00000471581.1:n.903+132delinsGT
NM_001256213.1:c.1026+132delinsGT	NP_001243142.1:n.1026+132delinsGT
NM_001256214.1:c.1032+132delinsGT	NP_001243143.1:n.1032+132delinsGT
NM_152296.4:c.993+132delinsGT	NP_689509.1:n.993+132delinsGT
XM_011526991.1:c.903+132delinsGT	XP_011525293.1:n.903+132delinsGT
NM_152296.5:c.993+132delinsGT MANE Select	NP_689509.1:n.993+132delinsGT
NM_001256214.2:c.1032+132delinsGT	NP_001243143.1:n.1032+132delinsGT
NM_001256213.2:c.1026+132delinsGT	NP_001243142.1:n.1026+132delinsGT