Canonical Allele Identifier: CA1202193016

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130606_160130607delinsCT , CM000663.2:g.160130606_160130607delinsCT	GRCh38
NC_000001.10:g.160100396_160100397delinsCT , CM000663.1:g.160100396_160100397delinsCT	GRCh37
NC_000001.9:g.158367020_158367021delinsCT	NCBI36
NG_008014.1:g.19849_19850delinsCT , LRG_6:g.19849_19850delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.1827+9_1827+10delinsCT MANE Select	ENSP00000354490.3:n.1827+9_1827+10delinsCT
ENST00000361216.7:c.1827+9_1827+10delinsCT	ENSP00000354490.3:n.1827+9_1827+10delinsCT
ENST00000392233.7:c.1827+9_1827+10delinsCT	ENSP00000376066.3:n.1827+9_1827+10delinsCT
ENST00000447527.1:c.959+9_959+10delinsCT
ENST00000472488.5:n.1930+9_1930+10delinsCT
NM_000702.3:c.1827+9_1827+10delinsCT	NP_000693.1:n.1827+9_1827+10delinsCT
NM_000702.4:c.1827+9_1827+10delinsCT MANE Select	NP_000693.1:n.1827+9_1827+10delinsCT