Canonical Allele Identifier: CA1665049261

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.133528844A= , CM000668.2:g.133528844A= GRCh38
NC_000006.11:g.133849982A= , CM000668.1:g.133849982A= GRCh37
NC_000006.10:g.133891675A= NCBI36
NG_011596.1:g.292488A=
NG_011596.2:g.292488A=

Transcript Alleles

HGVS Amino-acid change
ENST00000525849.7:c.*39A= (EYA4) ENSP00000433219.1:n.*39A=
ENST00000706301.1:c.*39A= (EYA4) ENSP00000516341.1:n.*39A=
ENST00000355167.8:c.*39A= (EYA4) ENSP00000347294.4:n.*39A=
ENST00000683325.1:c.*4141A= (EYA4) ENSP00000508141.1:n.*4141A=
ENST00000355286.12:c.*39A= (EYA4) MANE Select ENSP00000347434.7:n.*39A=
ENST00000431403.3:c.*39A= (EYA4) ENSP00000404558.3:n.*39A=
ENST00000525849.6:c.*39A= (EYA4) ENSP00000433219.1:n.*39A=
ENST00000355167.7:c.*39A= (EYA4) ENSP00000347294.3:n.*39A=
ENST00000355286.10:c.*39A= (EYA4) ENSP00000347434.6:n.*39A=
ENST00000367895.9:c.*39A= (EYA4) ENSP00000356870.5:n.*39A=
ENST00000430974.6:c.1696-2365A= (EYA4) ENSP00000388670.2:n.1696-2365A=
ENST00000431403.2:c.1959A= (EYA4) ENSP00000404558.2:n.1959A=
ENST00000452339.6:c.*39A= (EYA4) ENSP00000395916.2:n.*39A=
ENST00000525849.5:c.*39A= (EYA4) ENSP00000433219.1:n.*39A=
ENST00000531901.5:c.*39A= (EYA4) ENSP00000432770.1:n.*39A=
NM_001301012.1:c.*39A= (EYA4) NP_001287941.1:n.*39A=
NM_001301013.1:c.*39A= (EYA4) NP_001287942.1:n.*39A=
NM_004100.4:c.*39A= (EYA4) NP_004091.3:n.*39A=
NM_172103.3:c.*39A= (EYA4) NP_742101.2:n.*39A=
NM_172105.3:c.*39A= (EYA4) NP_742103.1:n.*39A=
NR_109982.1:n.2285+6936T= (TARID)
XM_005266851.3:c.*39A= (EYA4) XP_005266908.1:n.*39A=
XM_005266853.3:c.*39A= (EYA4) XP_005266910.1:n.*39A=
XM_011535540.1:c.1909A= (EYA4) XP_011533842.1:p.Ser637=
XM_011535541.1:c.1894A= (EYA4) XP_011533843.1:p.Ser632=
XM_011535542.1:c.1816A= (EYA4) XP_011533844.1:p.Ser606=
XM_005266851.5:c.*39A= (EYA4) XP_005266908.1:n.*39A=
XM_005266853.5:c.*39A= (EYA4) XP_005266910.1:n.*39A=
XM_017010368.2:c.*3482A= (EYA4) XP_016865857.1:n.*3482A=
XM_017010369.2:c.*3482A= (EYA4) XP_016865858.1:n.*3482A=
XM_017010370.2:c.*3482A= (EYA4) XP_016865859.1:n.*3482A=
XM_017010371.2:c.*3482A= (EYA4) XP_016865860.1:n.*3482A=
XM_017010372.2:c.*3482A= (EYA4) XP_016865861.1:n.*3482A=
XM_017010373.2:c.*3482A= (EYA4) XP_016865862.1:n.*3482A=
XM_017010374.2:c.*39A= (EYA4) XP_016865863.1:n.*39A=
XM_017010375.1:c.*39A= (EYA4) XP_016865864.1:n.*39A=
XR_001743220.2:n.5662A= (EYA4)
NM_004100.5:c.*39A= (EYA4) MANE Select NP_004091.3:n.*39A=
NM_001370458.1:c.*39A= (EYA4) NP_001357387.1:n.*39A=
NM_001370459.1:c.*39A= (EYA4) NP_001357388.1:n.*39A=
NM_001301012.2:c.*39A= (EYA4) NP_001287941.1:n.*39A=
NM_001301013.2:c.*39A= (EYA4) NP_001287942.1:n.*39A=
NM_172103.4:c.*39A= (EYA4) NP_742101.2:n.*39A=
NM_172105.4:c.*39A= (EYA4) NP_742103.1:n.*39A=