Canonical Allele Identifier: CA9467784

Gene: ATP1A3

Linked Data

• ClinVar Variation Id: 804553
• ClinVar RCV Id: RCV000991570 ; RCV002067590
• dbSNP Id: rs374578592
• ExAC: 19:42489334 C / T
• gnomAD v2: 19-42489334-C-T
• gnomAD v4: 19-41985182-C-T
• MyVariant Identifiers: chr19:g.42489334C>T (hg19) ; chr19:g.41985182C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985182C>T , CM000681.2:g.41985182C>T	GRCh38
NC_000019.9:g.42489334C>T , CM000681.1:g.42489334C>T	GRCh37
NC_000019.8:g.47181174C>T	NCBI36
NG_008015.1:g.14049G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.768G>A	ENSP00000444688.1:p.Thr256=
ENST00000644613.1:c.729G>A	ENSP00000494711.1:p.Thr243=
ENST00000648268.1:c.729G>A MANE Select	ENSP00000498113.1:p.Thr243=
ENST00000302102.9:c.729G>A	ENSP00000302397.5:p.Thr243=
ENST00000441343.5:c.729G>A	ENSP00000411503.1:p.Thr243=
ENST00000473086.3:c.639G>A	ENSP00000469129.2:p.Thr213=
ENST00000485672.2:n.42G>A
ENST00000543770.5:c.762G>A	ENSP00000437577.1:p.Thr254=
ENST00000545399.5:c.768G>A	ENSP00000444688.1:p.Thr256=
ENST00000602133.5:c.639G>A	ENSP00000471581.1:p.Thr213=
NM_001256213.1:c.762G>A	NP_001243142.1:p.Thr254=
NM_001256214.1:c.768G>A	NP_001243143.1:p.Thr256=
NM_152296.4:c.729G>A	NP_689509.1:p.Thr243=
XM_011526991.1:c.639G>A	XP_011525293.1:p.Thr213=
NM_152296.5:c.729G>A MANE Select	NP_689509.1:p.Thr243=
NM_001256214.2:c.768G>A	NP_001243143.1:p.Thr256=
NM_001256213.2:c.762G>A	NP_001243142.1:p.Thr254=