Canonical Allele Identifier: CA2585368863

Gene: ATP1A3

Linked Data

• gnomAD v4: 19-41970065-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41970067del , CM000681.2:g.41970067del	GRCh38
NC_000019.9:g.42474219del , CM000681.1:g.42474219del	GRCh37
NC_000019.8:g.47166059del	NCBI36
NG_008015.1:g.29165del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.2581+119del	ENSP00000444688.1:n.2581+119del
ENST00000644613.1:c.2542+119del	ENSP00000494711.1:n.2542+119del
ENST00000648268.1:c.2542+119del MANE Select	ENSP00000498113.1:n.2542+119del
ENST00000302102.9:c.2542+119del	ENSP00000302397.5:n.2542+119del
ENST00000441343.5:c.2542+119del	ENSP00000411503.1:n.2542+119del
ENST00000543770.5:c.2575+119del	ENSP00000437577.1:n.2575+119del
ENST00000545399.5:c.2581+119del	ENSP00000444688.1:n.2581+119del
ENST00000602133.5:c.2452+119del	ENSP00000471581.1:n.2452+119del
NM_001256213.1:c.2575+119del	NP_001243142.1:n.2575+119del
NM_001256214.1:c.2581+119del	NP_001243143.1:n.2581+119del
NM_152296.4:c.2542+119del	NP_689509.1:n.2542+119del
XM_011526991.1:c.2452+119del	XP_011525293.1:n.2452+119del
NM_152296.5:c.2542+119del MANE Select	NP_689509.1:n.2542+119del
NM_001256214.2:c.2581+119del	NP_001243143.1:n.2581+119del
NM_001256213.2:c.2575+119del	NP_001243142.1:n.2575+119del