Canonical Allele Identifier: CA1147856787
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139990C= , CM000663.2:g.160139990C= GRCh38
NC_000001.10:g.160109780C= , CM000663.1:g.160109780C= GRCh37
NC_000001.9:g.158376404C= NCBI36
NG_008014.1:g.29233C= , LRG_6:g.29233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.3034+6C= MANE Select ENSP00000354490.3:n.3034+6C=
ENST00000361216.7:c.3034+6C= ENSP00000354490.3:n.3034+6C=
ENST00000392233.7:c.3001+6C= ENSP00000376066.3:n.3001+6C=
ENST00000447527.1:c.2115+6C=
ENST00000459972.1:n.26+6C=
ENST00000463989.1:n.376C=
NM_000702.3:c.3034+6C= NP_000693.1:n.3034+6C=
NM_000702.4:c.3034+6C= MANE Select NP_000693.1:n.3034+6C=
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