Canonical Allele Identifier: CA1202196723

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160139335T= , CM000663.2:g.160139335T=	GRCh38
NC_000001.10:g.160109125T= , CM000663.1:g.160109125T=	GRCh37
NC_000001.9:g.158375749T=	NCBI36
NG_008014.1:g.28578T= , LRG_6:g.28578T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.2841-305T= MANE Select	ENSP00000354490.3:n.2841-305T=
ENST00000361216.7:c.2841-305T=	ENSP00000354490.3:n.2841-305T=
ENST00000392233.7:c.2841-305T=	ENSP00000376066.3:n.2841-305T=
ENST00000447527.1:c.1922-305T=
ENST00000463989.1:n.177-305T=
NM_000702.3:c.2841-305T=	NP_000693.1:n.2841-305T=
NM_000702.4:c.2841-305T= MANE Select	NP_000693.1:n.2841-305T=