Canonical Allele Identifier: CA1202196891
Gene: ATP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139766G= , CM000663.2:g.160139766G= GRCh38
NC_000001.10:g.160109556G= , CM000663.1:g.160109556G= GRCh37
NC_000001.9:g.158376180G= NCBI36
NG_008014.1:g.29009G= , LRG_6:g.29009G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.2942+25G= MANE Select ENSP00000354490.3:n.2942+25G=
ENST00000361216.7:c.2942+25G= ENSP00000354490.3:n.2942+25G=
ENST00000392233.7:c.2942+25G= ENSP00000376066.3:n.2942+25G=
ENST00000447527.1:c.2023+25G=
ENST00000463989.1:n.278+25G=
NM_000702.3:c.2942+25G= NP_000693.1:n.2942+25G=
NM_000702.4:c.2942+25G= MANE Select NP_000693.1:n.2942+25G=
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