Canonical Allele Identifier: CA343243927
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160100215T>G (hg19) chr1:g.160130425T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160130425T>G , CM000663.2:g.160130425T>G GRCh38
NC_000001.10:g.160100215T>G , CM000663.1:g.160100215T>G GRCh37
NC_000001.9:g.158366839T>G NCBI36
NG_008014.1:g.19668T>G , LRG_6:g.19668T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.1655T>G MANE Select ENSP00000354490.3:p.Phe552Cys
ENST00000361216.7:c.1655T>G ENSP00000354490.3:p.Phe552Cys
ENST00000392233.7:c.1655T>G ENSP00000376066.3:p.Phe552Cys
ENST00000447527.1:c.787T>G
ENST00000472488.5:n.1758T>G
NM_000702.3:c.1655T>G NP_000693.1:p.Phe552Cys
NM_000702.4:c.1655T>G MANE Select NP_000693.1:p.Phe552Cys
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