Canonical Allele Identifier: CA346032

Gene: ATP1A3

Linked Data

• ClinVar Variation Id: 161146
• ClinVar RCV Id: RCV002051815 ; RCV002273963
• dbSNP Id: rs606231442
• MyVariant Identifiers: chr19:g.42473675C>T (hg19) ; chr19:g.41969523C>T (hg38)
• PubMed: PMID:20301294

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41969523C>T , CM000681.2:g.41969523C>T	GRCh38
NC_000019.9:g.42473675C>T , CM000681.1:g.42473675C>T	GRCh37
NC_000019.8:g.47165515C>T	NCBI36
NG_008015.1:g.29708G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.2639G>A	ENSP00000444688.1:p.Gly880Asp
ENST00000644613.1:c.2600G>A	ENSP00000494711.1:p.Gly867Asp
ENST00000648268.1:c.2600G>A MANE Select	ENSP00000498113.1:p.Gly867Asp
ENST00000302102.9:c.2600G>A	ENSP00000302397.5:p.Gly867Asp
ENST00000441343.5:c.2600G>A	ENSP00000411503.1:p.Gly867Asp
ENST00000543770.5:c.2633G>A	ENSP00000437577.1:p.Gly878Asp
ENST00000545399.5:c.2639G>A	ENSP00000444688.1:p.Gly880Asp
ENST00000602133.5:c.2510G>A	ENSP00000471581.1:p.Gly837Asp
NM_001256213.1:c.2633G>A	NP_001243142.1:p.Gly878Asp
NM_001256214.1:c.2639G>A	NP_001243143.1:p.Gly880Asp
NM_152296.4:c.2600G>A	NP_689509.1:p.Gly867Asp
XM_011526991.1:c.2510G>A	XP_011525293.1:p.Gly837Asp
NM_152296.5:c.2600G>A MANE Select	NP_689509.1:p.Gly867Asp
NM_001256214.2:c.2639G>A	NP_001243143.1:p.Gly880Asp
NM_001256213.2:c.2633G>A	NP_001243142.1:p.Gly878Asp