Canonical Allele Identifier: CA1148974

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155688099A>G , CM000663.2:g.155688099A>G GRCh38
NC_000001.10:g.155657890A>G , CM000663.1:g.155657890A>G GRCh37
NC_000001.9:g.153924514A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_139119.3:c.-49T>C (YY1AP1) MANE Select NP_620830.1:n.-49T>C
ENST00000355499.9:c.-49T>C (YY1AP1) MANE Select ENSP00000347686.4:n.-49T>C
NM_001198900.1:c.-41T>C (YY1AP1) NP_001185829.1:n.-41T>C
NM_001198900.2:c.-41T>C (YY1AP1) NP_001185829.1:n.-41T>C
NM_001198901.1:c.-21+831T>C (YY1AP1) NP_001185830.1:n.-21+831T>C
NM_001198901.2:c.-21+831T>C (YY1AP1) NP_001185830.1:n.-21+831T>C
NM_001198902.1:c.-21+560T>C (YY1AP1) NP_001185831.1:n.-21+560T>C
NM_001198902.2:c.-21+560T>C (YY1AP1) NP_001185831.1:n.-21+560T>C
NM_001198903.1:c.366T>C (YY1AP1) NP_001185832.1:p.Cys122=
NM_001198904.1:c.366T>C (YY1AP1) NP_001185833.1:p.Cys122=
NM_001198905.1:c.-49T>C (YY1AP1) NP_001185834.1:n.-49T>C
NM_001198905.2:c.-49T>C (YY1AP1) NP_001185834.1:n.-49T>C
NM_001198906.1:c.150T>C (YY1AP1) NP_001185835.1:p.Cys50=
NM_001198906.2:c.150T>C (YY1AP1) NP_001185835.1:p.Cys50=
NM_018253.3:c.-163T>C (YY1AP1) NP_060723.2:n.-163T>C
NM_018253.4:c.-163T>C (YY1AP1) NP_060723.2:n.-163T>C
NM_139118.2:c.150T>C (YY1AP1) NP_620829.1:p.Cys50=
NM_139118.3:c.150T>C (YY1AP1) NP_620829.1:p.Cys50=
NM_139119.2:c.-49T>C (YY1AP1) NP_620830.1:n.-49T>C
NM_139121.2:c.-375+831T>C (YY1AP1) NP_620832.1:n.-375+831T>C
NM_139121.3:c.-375+831T>C (YY1AP1) NP_620832.1:n.-375+831T>C
ENST00000295566.8:c.150T>C (YY1AP1) ENSP00000295566.4:p.Cys50=
ENST00000311573.9:c.-116T>C (YY1AP1) ENSP00000311138.5:n.-116T>C
ENST00000347088.9:c.-21+560T>C (YY1AP1) ENSP00000316079.6:n.-21+560T>C
ENST00000354691.9:c.-49T>C (YY1AP1) ENSP00000346722.5:n.-49T>C
ENST00000355499.8:c.-49T>C (YY1AP1) ENSP00000347686.4:n.-49T>C
ENST00000359205.9:c.-41T>C (YY1AP1) ENSP00000352134.5:n.-41T>C
ENST00000361140.8:c.-49T>C (YY1AP1) ENSP00000354716.4:n.-49T>C
ENST00000361831.9:c.-163T>C (YY1AP1) ENSP00000355298.5:n.-163T>C
ENST00000368330.6:c.-21+831T>C (YY1AP1) ENSP00000357314.2:n.-21+831T>C
ENST00000368339.9:c.366T>C (YY1AP1) ENSP00000357323.5:p.Cys122=
ENST00000368340.9:c.366T>C (YY1AP1) ENSP00000357324.5:p.Cys122=
ENST00000404643.5:c.-49T>C (YY1AP1) ENSP00000385390.1:n.-49T>C
ENST00000405763.7:c.366T>C (YY1AP1) ENSP00000384583.3:p.Cys122=
ENST00000407221.5:c.-116T>C (YY1AP1) ENSP00000385791.1:n.-116T>C
ENST00000436865.5:c.-21+831T>C (YY1AP1) ENSP00000390116.1:n.-21+831T>C
ENST00000443231.5:c.-163T>C (YY1AP1) ENSP00000409203.1:n.-163T>C
ENST00000454523.5:c.-49T>C (YY1AP1) ENSP00000413240.1:n.-49T>C
ENST00000461479.1:n.140A>G (DAP3)
ENST00000471214.5:c.-274A>G (DAP3) ENSP00000476899.1:n.-274A>G
ENST00000471642.6:c.-181A>G (DAP3) ENSP00000476592.1:n.-181A>G
ENST00000476027.5:n.162T>C (YY1AP1)
ENST00000476093.5:n.46+831T>C (YY1AP1)
ENST00000479076.1:n.109A>G (DAP3)
XM_011509721.1:c.150T>C (YY1AP1) XP_011508023.1:p.Cys50=
XM_011509722.1:c.-41T>C (YY1AP1) XP_011508024.1:n.-41T>C
XM_024449697.1:c.-181A>G (DAP3) XP_024305465.1:n.-181A>G
XM_024449698.1:c.-181A>G (DAP3) XP_024305466.1:n.-181A>G