Canonical Allele Identifier: CA249413

Gene: ATP1A3

Linked Data

• ClinVar Variation Id: 218558
• ClinVar RCV Id: RCV001808560 ; RCV003765310
• dbSNP Id: rs864309572
• MyVariant Identifiers: chr19:g.42489096G>A (hg19) ; chr19:g.41984944G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41984944G>A , CM000681.2:g.41984944G>A	GRCh38
NC_000019.9:g.42489096G>A , CM000681.1:g.42489096G>A	GRCh37
NC_000019.8:g.47180936G>A	NCBI36
NG_008015.1:g.14287C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000545399.6:c.1006C>T	ENSP00000444688.1:p.Pro336Ser
ENST00000644613.1:c.967C>T	ENSP00000494711.1:p.Pro323Ser
ENST00000648268.1:c.967C>T MANE Select	ENSP00000498113.1:p.Pro323Ser
ENST00000302102.9:c.967C>T	ENSP00000302397.5:p.Pro323Ser
ENST00000441343.5:c.967C>T	ENSP00000411503.1:p.Pro323Ser
ENST00000485672.2:n.280C>T
ENST00000543770.5:c.1000C>T	ENSP00000437577.1:p.Pro334Ser
ENST00000545399.5:c.1006C>T	ENSP00000444688.1:p.Pro336Ser
ENST00000602133.5:c.877C>T	ENSP00000471581.1:p.Pro293Ser
NM_001256213.1:c.1000C>T	NP_001243142.1:p.Pro334Ser
NM_001256214.1:c.1006C>T	NP_001243143.1:p.Pro336Ser
NM_152296.4:c.967C>T	NP_689509.1:p.Pro323Ser
XM_011526991.1:c.877C>T	XP_011525293.1:p.Pro293Ser
NM_152296.5:c.967C>T MANE Select	NP_689509.1:p.Pro323Ser
NM_001256214.2:c.1006C>T	NP_001243143.1:p.Pro336Ser
NM_001256213.2:c.1000C>T	NP_001243142.1:p.Pro334Ser