Canonical Allele Identifier: CA1665049218

Gene: EYA4 TARID

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133528829_133528830delinsAT , CM000668.2:g.133528829_133528830delinsAT	GRCh38
NC_000006.11:g.133849967_133849968delinsAT , CM000668.1:g.133849967_133849968delinsAT	GRCh37
NC_000006.10:g.133891660_133891661delinsAT	NCBI36
NG_011596.1:g.292473_292474delinsAT
NG_011596.2:g.292473_292474delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000525849.7:c.*24_*25delinsAT (EYA4)	ENSP00000433219.1:n.*24_*25delinsAT
ENST00000706301.1:c.*24_*25delinsAT (EYA4)	ENSP00000516341.1:n.*24_*25delinsAT
ENST00000355167.8:c.*24_*25delinsAT (EYA4)	ENSP00000347294.4:n.*24_*25delinsAT
ENST00000683325.1:c.*4126_*4127delinsAT (EYA4)	ENSP00000508141.1:n.*4126_*4127delinsAT
ENST00000355286.12:c.*24_*25delinsAT (EYA4) MANE Select	ENSP00000347434.7:n.*24_*25delinsAT
ENST00000431403.3:c.*24_*25delinsAT (EYA4)	ENSP00000404558.3:n.*24_*25delinsAT
ENST00000525849.6:c.*24_*25delinsAT (EYA4)	ENSP00000433219.1:n.*24_*25delinsAT
ENST00000355167.7:c.*24_*25delinsAT (EYA4)	ENSP00000347294.3:n.*24_*25delinsAT
ENST00000355286.10:c.*24_*25delinsAT (EYA4)	ENSP00000347434.6:n.*24_*25delinsAT
ENST00000367895.9:c.*24_*25delinsAT (EYA4)	ENSP00000356870.5:n.*24_*25delinsAT
ENST00000430974.6:c.1696-2380_1696-2379delinsAT (EYA4)	ENSP00000388670.2:n.1696-2380_1696-2379delinsAT
ENST00000431403.2:c.1944_1945delinsAT (EYA4)	ENSP00000404558.2:n.1944_1945delinsAT
ENST00000452339.6:c.*24_*25delinsAT (EYA4)	ENSP00000395916.2:n.*24_*25delinsAT
ENST00000525849.5:c.*24_*25delinsAT (EYA4)	ENSP00000433219.1:n.*24_*25delinsAT
ENST00000531901.5:c.*24_*25delinsAT (EYA4)	ENSP00000432770.1:n.*24_*25delinsAT
NM_001301012.1:c.*24_*25delinsAT (EYA4)	NP_001287941.1:n.*24_*25delinsAT
NM_001301013.1:c.*24_*25delinsAT (EYA4)	NP_001287942.1:n.*24_*25delinsAT
NM_004100.4:c.*24_*25delinsAT (EYA4)	NP_004091.3:n.*24_*25delinsAT
NM_172103.3:c.*24_*25delinsAT (EYA4)	NP_742101.2:n.*24_*25delinsAT
NM_172105.3:c.*24_*25delinsAT (EYA4)	NP_742103.1:n.*24_*25delinsAT
NR_109982.1:n.2285+6950_2285+6951delinsAT (TARID)
XM_005266851.3:c.*24_*25delinsAT (EYA4)	XP_005266908.1:n.*24_*25delinsAT
XM_005266853.3:c.*24_*25delinsAT (EYA4)	XP_005266910.1:n.*24_*25delinsAT
XM_011535540.1:c.1894_1895delinsAT (EYA4)	XP_011533842.1:p.Ile632=
XM_011535541.1:c.1879_1880delinsAT (EYA4)	XP_011533843.1:p.Ile627=
XM_011535542.1:c.1801_1802delinsAT (EYA4)	XP_011533844.1:p.Ile601=
XM_005266851.5:c.*24_*25delinsAT (EYA4)	XP_005266908.1:n.*24_*25delinsAT
XM_005266853.5:c.*24_*25delinsAT (EYA4)	XP_005266910.1:n.*24_*25delinsAT
XM_017010368.2:c.*3467_*3468delinsAT (EYA4)	XP_016865857.1:n.*3467_*3468delinsAT
XM_017010369.2:c.*3467_*3468delinsAT (EYA4)	XP_016865858.1:n.*3467_*3468delinsAT
XM_017010370.2:c.*3467_*3468delinsAT (EYA4)	XP_016865859.1:n.*3467_*3468delinsAT
XM_017010371.2:c.*3467_*3468delinsAT (EYA4)	XP_016865860.1:n.*3467_*3468delinsAT
XM_017010372.2:c.*3467_*3468delinsAT (EYA4)	XP_016865861.1:n.*3467_*3468delinsAT
XM_017010373.2:c.*3467_*3468delinsAT (EYA4)	XP_016865862.1:n.*3467_*3468delinsAT
XM_017010374.2:c.*24_*25delinsAT (EYA4)	XP_016865863.1:n.*24_*25delinsAT
XM_017010375.1:c.*24_*25delinsAT (EYA4)	XP_016865864.1:n.*24_*25delinsAT
XR_001743220.2:n.5647_5648delinsAT (EYA4)
NM_004100.5:c.*24_*25delinsAT (EYA4) MANE Select	NP_004091.3:n.*24_*25delinsAT
NM_001370458.1:c.*24_*25delinsAT (EYA4)	NP_001357387.1:n.*24_*25delinsAT
NM_001370459.1:c.*24_*25delinsAT (EYA4)	NP_001357388.1:n.*24_*25delinsAT
NM_001301012.2:c.*24_*25delinsAT (EYA4)	NP_001287941.1:n.*24_*25delinsAT
NM_001301013.2:c.*24_*25delinsAT (EYA4)	NP_001287942.1:n.*24_*25delinsAT
NM_172103.4:c.*24_*25delinsAT (EYA4)	NP_742101.2:n.*24_*25delinsAT
NM_172105.4:c.*24_*25delinsAT (EYA4)	NP_742103.1:n.*24_*25delinsAT