Canonical Allele Identifier: CA1202192946

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130364_160130365delinsTG , CM000663.2:g.160130364_160130365delinsTG	GRCh38
NC_000001.10:g.160100154_160100155delinsTG , CM000663.1:g.160100154_160100155delinsTG	GRCh37
NC_000001.9:g.158366778_158366779delinsTG	NCBI36
NG_008014.1:g.19607_19608delinsTG , LRG_6:g.19607_19608delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.1652-58_1652-57delinsTG MANE Select	ENSP00000354490.3:n.1652-58_1652-57delinsTG
ENST00000361216.7:c.1652-58_1652-57delinsTG	ENSP00000354490.3:n.1652-58_1652-57delinsTG
ENST00000392233.7:c.1652-58_1652-57delinsTG	ENSP00000376066.3:n.1652-58_1652-57delinsTG
ENST00000447527.1:c.784-58_784-57delinsTG
ENST00000472488.5:n.1755-58_1755-57delinsTG
NM_000702.3:c.1652-58_1652-57delinsTG	NP_000693.1:n.1652-58_1652-57delinsTG
NM_000702.4:c.1652-58_1652-57delinsTG MANE Select	NP_000693.1:n.1652-58_1652-57delinsTG