Canonical Allele Identifier: CA406052665

Gene: ATP1A3

Linked Data

• MyVariant Identifiers: chr19:g.42489189G>T (hg19) ; chr19:g.41985037G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41985037G>T , CM000681.2:g.41985037G>T	GRCh38
NC_000019.9:g.42489189G>T , CM000681.1:g.42489189G>T	GRCh37
NC_000019.8:g.47181029G>T	NCBI36
NG_008015.1:g.14194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000545399.6:c.913C>A	ENSP00000444688.1:p.Leu305Met
ENST00000644613.1:c.874C>A	ENSP00000494711.1:p.Leu292Met
ENST00000648268.1:c.874C>A MANE Select	ENSP00000498113.1:p.Leu292Met
ENST00000302102.9:c.874C>A	ENSP00000302397.5:p.Leu292Met
ENST00000441343.5:c.874C>A	ENSP00000411503.1:p.Leu292Met
ENST00000485672.2:n.187C>A
ENST00000543770.5:c.907C>A	ENSP00000437577.1:p.Leu303Met
ENST00000545399.5:c.913C>A	ENSP00000444688.1:p.Leu305Met
ENST00000602133.5:c.784C>A	ENSP00000471581.1:p.Leu262Met
NM_001256213.1:c.907C>A	NP_001243142.1:p.Leu303Met
NM_001256214.1:c.913C>A	NP_001243143.1:p.Leu305Met
NM_152296.4:c.874C>A	NP_689509.1:p.Leu292Met
XM_011526991.1:c.784C>A	XP_011525293.1:p.Leu262Met
NM_152296.5:c.874C>A MANE Select	NP_689509.1:p.Leu292Met
NM_001256214.2:c.913C>A	NP_001243143.1:p.Leu305Met
NM_001256213.2:c.907C>A	NP_001243142.1:p.Leu303Met