Canonical Allele Identifier: CA1202191855

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160127602C= , CM000663.2:g.160127602C=	GRCh38
NC_000001.10:g.160097392C= , CM000663.1:g.160097392C=	GRCh37
NC_000001.9:g.158364016C=	NCBI36
NG_008014.1:g.16845C= , LRG_6:g.16845C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.799C= MANE Select	ENSP00000354490.3:p.Arg267=
ENST00000361216.7:c.799C=	ENSP00000354490.3:p.Arg267=
ENST00000392233.7:c.799C=	ENSP00000376066.3:p.Arg267=
ENST00000472488.5:n.902C=
NM_000702.3:c.799C=	NP_000693.1:p.Arg267=
NM_000702.4:c.799C= MANE Select	NP_000693.1:p.Arg267=