Canonical Allele Identifier: CA2680407921

Gene: EYA4 TARID

Linked Data

• gnomAD v4: 6-133530324-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133530324_133530325insC , CM000668.2:g.133530324_133530325insC	GRCh38
NC_000006.11:g.133851462_133851463insC , CM000668.1:g.133851462_133851463insC	GRCh37
NC_000006.10:g.133893155_133893156insC	NCBI36
NG_011596.1:g.293968_293969insC
NG_011596.2:g.293968_293969insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525849.7:c.*1519_*1520insC (EYA4)	ENSP00000433219.1:n.*1519_*1520insC
ENST00000706301.1:c.*1519_*1520insC (EYA4)	ENSP00000516341.1:n.*1519_*1520insC
ENST00000355167.8:c.*1519_*1520insC (EYA4)	ENSP00000347294.4:n.*1519_*1520insC
ENST00000355286.12:c.*1519_*1520insC (EYA4) MANE Select	ENSP00000347434.7:n.*1519_*1520insC
ENST00000355167.7:c.*1519_*1520insC (EYA4)	ENSP00000347294.3:n.*1519_*1520insC
ENST00000355286.10:c.*1519_*1520insC (EYA4)	ENSP00000347434.6:n.*1519_*1520insC
ENST00000367895.9:c.*1519_*1520insC (EYA4)	ENSP00000356870.5:n.*1519_*1520insC
ENST00000430974.6:c.1696-885_1696-884insC (EYA4)	ENSP00000388670.2:n.1696-885_1696-884insC
NM_001301012.1:c.*1519_*1520insC (EYA4)	NP_001287941.1:n.*1519_*1520insC
NM_001301013.1:c.*1519_*1520insC (EYA4)	NP_001287942.1:n.*1519_*1520insC
NM_004100.4:c.*1519_*1520insC (EYA4)	NP_004091.3:n.*1519_*1520insC
NM_172103.3:c.*1519_*1520insC (EYA4)	NP_742101.2:n.*1519_*1520insC
NM_172105.3:c.*1519_*1520insC (EYA4)	NP_742103.1:n.*1519_*1520insC
NR_109982.1:n.2285+5455_2285+5456insG (TARID)
XM_005266851.3:c.*1519_*1520insC (EYA4)	XP_005266908.1:n.*1519_*1520insC
XM_005266853.3:c.*1519_*1520insC (EYA4)	XP_005266910.1:n.*1519_*1520insC
XM_011535540.1:c.*1457_*1458insC (EYA4)	XP_011533842.1:n.*1457_*1458insC
XM_011535541.1:c.*1457_*1458insC (EYA4)	XP_011533843.1:n.*1457_*1458insC
XM_011535542.1:c.*1457_*1458insC (EYA4)	XP_011533844.1:n.*1457_*1458insC
XM_005266851.5:c.*1519_*1520insC (EYA4)	XP_005266908.1:n.*1519_*1520insC
XM_005266853.5:c.*1519_*1520insC (EYA4)	XP_005266910.1:n.*1519_*1520insC
XM_017010368.2:c.*4962_*4963insC (EYA4)	XP_016865857.1:n.*4962_*4963insC
XM_017010369.2:c.*4962_*4963insC (EYA4)	XP_016865858.1:n.*4962_*4963insC
XM_017010370.2:c.*4962_*4963insC (EYA4)	XP_016865859.1:n.*4962_*4963insC
XM_017010371.2:c.*4962_*4963insC (EYA4)	XP_016865860.1:n.*4962_*4963insC
XM_017010372.2:c.*4962_*4963insC (EYA4)	XP_016865861.1:n.*4962_*4963insC
XM_017010373.2:c.*4962_*4963insC (EYA4)	XP_016865862.1:n.*4962_*4963insC
XM_017010374.2:c.*1519_*1520insC (EYA4)	XP_016865863.1:n.*1519_*1520insC
XM_017010375.1:c.*1519_*1520insC (EYA4)	XP_016865864.1:n.*1519_*1520insC
XR_001743220.2:n.7142_7143insC (EYA4)
NM_004100.5:c.*1519_*1520insC (EYA4) MANE Select	NP_004091.3:n.*1519_*1520insC
NM_001370458.1:c.*1519_*1520insC (EYA4)	NP_001357387.1:n.*1519_*1520insC
NM_001370459.1:c.*1519_*1520insC (EYA4)	NP_001357388.1:n.*1519_*1520insC
NM_001301012.2:c.*1519_*1520insC (EYA4)	NP_001287941.1:n.*1519_*1520insC
NM_001301013.2:c.*1519_*1520insC (EYA4)	NP_001287942.1:n.*1519_*1520insC
NM_172103.4:c.*1519_*1520insC (EYA4)	NP_742101.2:n.*1519_*1520insC
NM_172105.4:c.*1519_*1520insC (EYA4)	NP_742103.1:n.*1519_*1520insC