Canonical Allele Identifier: CA1202193058
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130679A= , CM000663.2:g.160130679A= GRCh38
NC_000001.10:g.160100469A= , CM000663.1:g.160100469A= GRCh37
NC_000001.9:g.158367093A= NCBI36
NG_008014.1:g.19922A= , LRG_6:g.19922A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1827+82A= MANE Select ENSP00000354490.3:n.1827+82A=
ENST00000361216.7:c.1827+82A= ENSP00000354490.3:n.1827+82A=
ENST00000392233.7:c.1827+82A= ENSP00000376066.3:n.1827+82A=
ENST00000447527.1:c.959+82A=
ENST00000472488.5:n.1930+82A=
NM_000702.3:c.1827+82A= NP_000693.1:n.1827+82A=
NM_000702.4:c.1827+82A= MANE Select NP_000693.1:n.1827+82A=
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