Canonical Allele Identifier: CA406039787

Gene: ATP1A3

Linked Data

• ClinVar Variation Id: 1705555
• ClinVar RCV Id: RCV002283869
• MyVariant Identifiers: chr19:g.42474692G>T (hg19) ; chr19:g.41970540G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41970540G>T , CM000681.2:g.41970540G>T	GRCh38
NC_000019.9:g.42474692G>T , CM000681.1:g.42474692G>T	GRCh37
NC_000019.8:g.47166532G>T	NCBI36
NG_008015.1:g.28691C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.2305C>A	ENSP00000444688.1:p.Arg769Ser
ENST00000644613.1:c.2266C>A	ENSP00000494711.1:p.Arg756Ser
ENST00000648268.1:c.2266C>A MANE Select	ENSP00000498113.1:p.Arg756Ser
ENST00000302102.9:c.2266C>A	ENSP00000302397.5:p.Arg756Ser
ENST00000441343.5:c.2266C>A	ENSP00000411503.1:p.Arg756Ser
ENST00000543770.5:c.2299C>A	ENSP00000437577.1:p.Arg767Ser
ENST00000545399.5:c.2305C>A	ENSP00000444688.1:p.Arg769Ser
ENST00000602133.5:c.2176C>A	ENSP00000471581.1:p.Arg726Ser
NM_001256213.1:c.2299C>A	NP_001243142.1:p.Arg767Ser
NM_001256214.1:c.2305C>A	NP_001243143.1:p.Arg769Ser
NM_152296.4:c.2266C>A	NP_689509.1:p.Arg756Ser
XM_011526991.1:c.2176C>A	XP_011525293.1:p.Arg726Ser
NM_152296.5:c.2266C>A MANE Select	NP_689509.1:p.Arg756Ser
NM_001256214.2:c.2305C>A	NP_001243143.1:p.Arg769Ser
NM_001256213.2:c.2299C>A	NP_001243142.1:p.Arg767Ser