Canonical Allele Identifier: CA406055771

Gene: ATP1A3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41986230C>T , CM000681.2:g.41986230C>T	GRCh38
NC_000019.9:g.42490382C>T , CM000681.1:g.42490382C>T	GRCh37
NC_000019.8:g.47182222C>T	NCBI36
NG_008015.1:g.13001G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_152296.5:c.358-1G>A MANE Select	NP_689509.1:n.358-1G>A
ENST00000648268.1:c.358-1G>A MANE Select	ENSP00000498113.1:n.358-1G>A
NM_001256213.1:c.391-1G>A	NP_001243142.1:n.391-1G>A
NM_001256213.2:c.391-1G>A	NP_001243142.1:n.391-1G>A
NM_001256214.1:c.397-1G>A	NP_001243143.1:n.397-1G>A
NM_001256214.2:c.397-1G>A	NP_001243143.1:n.397-1G>A
NM_152296.4:c.358-1G>A	NP_689509.1:n.358-1G>A
ENST00000302102.9:c.358-1G>A	ENSP00000302397.5:n.358-1G>A
ENST00000441343.5:c.358-1G>A	ENSP00000411503.1:n.358-1G>A
ENST00000473086.3:c.268-1G>A	ENSP00000469129.2:n.268-1G>A
ENST00000543770.5:c.391-1G>A	ENSP00000437577.1:n.391-1G>A
ENST00000545399.5:c.397-1G>A	ENSP00000444688.1:n.397-1G>A
ENST00000545399.6:c.397-1G>A	ENSP00000444688.1:n.397-1G>A
ENST00000602133.5:c.268-1G>A	ENSP00000471581.1:n.268-1G>A
ENST00000644613.1:c.358-1G>A	ENSP00000494711.1:n.358-1G>A
ENST00000645448.1:n.472G>A
XM_011526991.1:c.268-1G>A	XP_011525293.1:n.268-1G>A