Canonical Allele Identifier: CA1143372935

Gene: ATP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160130431A= , CM000663.2:g.160130431A=	GRCh38
NC_000001.10:g.160100221A= , CM000663.1:g.160100221A=	GRCh37
NC_000001.9:g.158366845A=	NCBI36
NG_008014.1:g.19674A= , LRG_6:g.19674A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361216.8:c.1661A= MANE Select	ENSP00000354490.3:p.Gln554=
ENST00000361216.7:c.1661A=	ENSP00000354490.3:p.Gln554=
ENST00000392233.7:c.1661A=	ENSP00000376066.3:p.Gln554=
ENST00000447527.1:c.793A=
ENST00000472488.5:n.1764A=
NM_000702.3:c.1661A=	NP_000693.1:p.Gln554=
NM_000702.4:c.1661A= MANE Select	NP_000693.1:p.Gln554=