Canonical Allele Identifier: CA343256603
Gene: ATP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.160109753A>G (hg19) chr1:g.160139963A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.160139963A>G , CM000663.2:g.160139963A>G GRCh38
NC_000001.10:g.160109753A>G , CM000663.1:g.160109753A>G GRCh37
NC_000001.9:g.158376377A>G NCBI36
NG_008014.1:g.29206A>G , LRG_6:g.29206A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361216.8:c.3013A>G MANE Select ENSP00000354490.3:p.Ile1005Val
ENST00000361216.7:c.3013A>G ENSP00000354490.3:p.Ile1005Val
ENST00000392233.7:c.2980A>G ENSP00000376066.3:p.Ile994Val
ENST00000447527.1:c.2094A>G
ENST00000459972.1:n.5A>G
ENST00000463989.1:n.349A>G
NM_000702.3:c.3013A>G NP_000693.1:p.Ile1005Val
NM_000702.4:c.3013A>G MANE Select NP_000693.1:p.Ile1005Val
Search 100 bp 5'
Search 100 bp 3'