Canonical Allele Identifier: CA1143366021
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160127530C= , CM000663.2:g.160127530C= GRCh38
NC_000001.10:g.160097320C= , CM000663.1:g.160097320C= GRCh37
NC_000001.9:g.158363944C= NCBI36
NG_008014.1:g.16773C= , LRG_6:g.16773C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.749-22C= MANE Select ENSP00000354490.3:n.749-22C=
ENST00000361216.7:c.749-22C= ENSP00000354490.3:n.749-22C=
ENST00000392233.7:c.749-22C= ENSP00000376066.3:n.749-22C=
ENST00000472488.5:n.852-22C=
NM_000702.3:c.749-22C= NP_000693.1:n.749-22C=
NM_000702.4:c.749-22C= MANE Select NP_000693.1:n.749-22C=
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