Canonical Allele Identifier: CA882390672

Gene: ATP1A3

Linked Data

• dbSNP Id: rs1292889445
• MyVariant Identifiers: chr19:g.41982112G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41982112G>A , CM000681.2:g.41982112G>A	GRCh38
NC_000019.9:g.42486264G>A , CM000681.1:g.42486264G>A	GRCh37
NC_000019.8:g.47178104G>A	NCBI36
NG_008015.1:g.17119C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000545399.6:c.1033-6C>T	ENSP00000444688.1:n.1033-6C>T
ENST00000644613.1:c.994-6C>T	ENSP00000494711.1:n.994-6C>T
ENST00000648268.1:c.994-6C>T MANE Select	ENSP00000498113.1:n.994-6C>T
ENST00000302102.9:c.994-6C>T	ENSP00000302397.5:n.994-6C>T
ENST00000441343.5:c.994-6C>T	ENSP00000411503.1:n.994-6C>T
ENST00000543770.5:c.1027-6C>T	ENSP00000437577.1:n.1027-6C>T
ENST00000545399.5:c.1033-6C>T	ENSP00000444688.1:n.1033-6C>T
ENST00000602133.5:c.904-6C>T	ENSP00000471581.1:n.904-6C>T
NM_001256213.1:c.1027-6C>T	NP_001243142.1:n.1027-6C>T
NM_001256214.1:c.1033-6C>T	NP_001243143.1:n.1033-6C>T
NM_152296.4:c.994-6C>T	NP_689509.1:n.994-6C>T
XM_011526991.1:c.904-6C>T	XP_011525293.1:n.904-6C>T
NM_152296.5:c.994-6C>T MANE Select	NP_689509.1:n.994-6C>T
NM_001256214.2:c.1033-6C>T	NP_001243143.1:n.1033-6C>T
NM_001256213.2:c.1027-6C>T	NP_001243142.1:n.1027-6C>T