Canonical Allele Identifier: CA1665049272

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133528848C= , CM000668.2:g.133528848C= GRCh38
NC_000006.11:g.133849986C= , CM000668.1:g.133849986C= GRCh37
NC_000006.10:g.133891679C= NCBI36
NG_011596.1:g.292492C=
NG_011596.2:g.292492C=

Transcript Alleles

HGVS Amino-acid change
ENST00000525849.7:c.*43C= (EYA4) ENSP00000433219.1:n.*43C=
ENST00000706301.1:c.*43C= (EYA4) ENSP00000516341.1:n.*43C=
ENST00000355167.8:c.*43C= (EYA4) ENSP00000347294.4:n.*43C=
ENST00000683325.1:c.*4145C= (EYA4) ENSP00000508141.1:n.*4145C=
ENST00000355286.12:c.*43C= (EYA4) MANE Select ENSP00000347434.7:n.*43C=
ENST00000431403.3:c.*43C= (EYA4) ENSP00000404558.3:n.*43C=
ENST00000525849.6:c.*43C= (EYA4) ENSP00000433219.1:n.*43C=
ENST00000355167.7:c.*43C= (EYA4) ENSP00000347294.3:n.*43C=
ENST00000355286.10:c.*43C= (EYA4) ENSP00000347434.6:n.*43C=
ENST00000367895.9:c.*43C= (EYA4) ENSP00000356870.5:n.*43C=
ENST00000430974.6:c.1696-2361C= (EYA4) ENSP00000388670.2:n.1696-2361C=
ENST00000431403.2:c.1963C= (EYA4) ENSP00000404558.2:n.1963C=
ENST00000452339.6:c.*43C= (EYA4) ENSP00000395916.2:n.*43C=
ENST00000525849.5:c.*43C= (EYA4) ENSP00000433219.1:n.*43C=
ENST00000531901.5:c.*43C= (EYA4) ENSP00000432770.1:n.*43C=
NM_001301012.1:c.*43C= (EYA4) NP_001287941.1:n.*43C=
NM_001301013.1:c.*43C= (EYA4) NP_001287942.1:n.*43C=
NM_004100.4:c.*43C= (EYA4) NP_004091.3:n.*43C=
NM_172103.3:c.*43C= (EYA4) NP_742101.2:n.*43C=
NM_172105.3:c.*43C= (EYA4) NP_742103.1:n.*43C=
NR_109982.1:n.2285+6932G= (TARID)
XM_005266851.3:c.*43C= (EYA4) XP_005266908.1:n.*43C=
XM_005266853.3:c.*43C= (EYA4) XP_005266910.1:n.*43C=
XM_011535540.1:c.1913C= (EYA4) XP_011533842.1:p.Thr638=
XM_011535541.1:c.1898C= (EYA4) XP_011533843.1:p.Thr633=
XM_011535542.1:c.1820C= (EYA4) XP_011533844.1:p.Thr607=
XM_005266851.5:c.*43C= (EYA4) XP_005266908.1:n.*43C=
XM_005266853.5:c.*43C= (EYA4) XP_005266910.1:n.*43C=
XM_017010368.2:c.*3486C= (EYA4) XP_016865857.1:n.*3486C=
XM_017010369.2:c.*3486C= (EYA4) XP_016865858.1:n.*3486C=
XM_017010370.2:c.*3486C= (EYA4) XP_016865859.1:n.*3486C=
XM_017010371.2:c.*3486C= (EYA4) XP_016865860.1:n.*3486C=
XM_017010372.2:c.*3486C= (EYA4) XP_016865861.1:n.*3486C=
XM_017010373.2:c.*3486C= (EYA4) XP_016865862.1:n.*3486C=
XM_017010374.2:c.*43C= (EYA4) XP_016865863.1:n.*43C=
XM_017010375.1:c.*43C= (EYA4) XP_016865864.1:n.*43C=
XR_001743220.2:n.5666C= (EYA4)
NM_004100.5:c.*43C= (EYA4) MANE Select NP_004091.3:n.*43C=
NM_001370458.1:c.*43C= (EYA4) NP_001357387.1:n.*43C=
NM_001370459.1:c.*43C= (EYA4) NP_001357388.1:n.*43C=
NM_001301012.2:c.*43C= (EYA4) NP_001287941.1:n.*43C=
NM_001301013.2:c.*43C= (EYA4) NP_001287942.1:n.*43C=
NM_172103.4:c.*43C= (EYA4) NP_742101.2:n.*43C=
NM_172105.4:c.*43C= (EYA4) NP_742103.1:n.*43C=