Canonical Allele Identifier: CA1202192913
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130298G= , CM000663.2:g.160130298G= GRCh38
NC_000001.10:g.160100088G= , CM000663.1:g.160100088G= GRCh37
NC_000001.9:g.158366712G= NCBI36
NG_008014.1:g.19541G= , LRG_6:g.19541G=

Transcript Alleles

HGVS Amino-acid change
ENST00000361216.8:c.1651+7G= MANE Select ENSP00000354490.3:n.1651+7G=
ENST00000361216.7:c.1651+7G= ENSP00000354490.3:n.1651+7G=
ENST00000392233.7:c.1651+7G= ENSP00000376066.3:n.1651+7G=
ENST00000447527.1:c.783+7G=
ENST00000472488.5:n.1754+7G=
NM_000702.3:c.1651+7G= NP_000693.1:n.1651+7G=
NM_000702.4:c.1651+7G= MANE Select NP_000693.1:n.1651+7G=
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