Canonical Allele Identifier: CA31350463
Community Standard Title: NM_001319658.2(DUSP23):c.364A>G (p.Ile122Val)
Gene: DUSP23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159782249A>G , CM000663.2:g.159782249A>G GRCh38
NC_000001.10:g.159752039A>G , CM000663.1:g.159752039A>G GRCh37
NC_000001.9:g.158018663A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001319658.2:c.364A>G MANE Select NP_001306587.1:p.Ile122Val
ENST00000368107.2:c.364A>G MANE Select ENSP00000357087.1:p.Ile122Val
NM_001319658.1:c.364A>G NP_001306587.1:p.Ile122Val
NM_001319659.1:c.364A>G NP_001306588.1:p.Ile122Val
NM_001319659.2:c.364A>G NP_001306588.1:p.Ile122Val
NM_017823.3:c.364A>G NP_060293.2:p.Ile122Val
NM_017823.4:c.364A>G NP_060293.2:p.Ile122Val
NM_017823.5:c.364A>G NP_060293.2:p.Ile122Val
ENST00000368107.1:c.364A>G ENSP00000357087.1:p.Ile122Val
ENST00000368108.7:c.364A>G ENSP00000357088.3:p.Ile122Val
ENST00000368109.5:c.364A>G ENSP00000357089.1:p.Ile122Val
XM_005245289.1:c.364A>G XP_005245346.1:p.Ile122Val