Canonical Allele Identifier: CA365698292

Gene: EYA4 TARID

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133523064G>A , CM000668.2:g.133523064G>A	GRCh38
NC_000006.11:g.133844202G>A , CM000668.1:g.133844202G>A	GRCh37
NC_000006.10:g.133885895G>A	NCBI36
NG_011596.1:g.286708G>A
NG_011596.2:g.286708G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004100.5:c.1625G>A (EYA4) MANE Select	NP_004091.3:p.Cys542Tyr
ENST00000355286.12:c.1625G>A (EYA4) MANE Select	ENSP00000347434.7:p.Cys542Tyr
NM_001301012.1:c.1463G>A (EYA4)	NP_001287941.1:p.Cys488Tyr
NM_001301012.2:c.1463G>A (EYA4)	NP_001287941.1:p.Cys488Tyr
NM_001301013.1:c.1643G>A (EYA4)	NP_001287942.1:p.Cys548Tyr
NM_001301013.2:c.1643G>A (EYA4)	NP_001287942.1:p.Cys548Tyr
NM_001370458.1:c.1556G>A (EYA4)	NP_001357387.1:p.Cys519Tyr
NM_001370459.1:c.1481G>A (EYA4)	NP_001357388.1:p.Cys494Tyr
NM_004100.4:c.1625G>A (EYA4)	NP_004091.3:p.Cys542Tyr
NM_172103.3:c.1556G>A (EYA4)	NP_742101.2:p.Cys519Tyr
NM_172103.4:c.1556G>A (EYA4)	NP_742101.2:p.Cys519Tyr
NM_172105.3:c.1625G>A (EYA4)	NP_742103.1:p.Cys542Tyr
NM_172105.4:c.1625G>A (EYA4)	NP_742103.1:p.Cys542Tyr
NR_109982.1:n.2285+12716C>T (TARID)
ENST00000355167.7:c.1625G>A (EYA4)	ENSP00000347294.3:p.Cys542Tyr
ENST00000355167.8:c.1481G>A (EYA4)	ENSP00000347294.4:p.Cys494Tyr
ENST00000355286.10:c.1556G>A (EYA4)	ENSP00000347434.6:p.Cys519Tyr
ENST00000367895.9:c.1625G>A (EYA4)	ENSP00000356870.5:p.Cys542Tyr
ENST00000430974.6:c.1481G>A (EYA4)	ENSP00000388670.2:p.Cys494Tyr
ENST00000431403.2:c.1625G>A (EYA4)	ENSP00000404558.2:p.Cys542Tyr
ENST00000431403.3:c.1556G>A (EYA4)	ENSP00000404558.3:p.Cys519Tyr
ENST00000452339.6:c.1463G>A (EYA4)	ENSP00000395916.2:p.Cys488Tyr
ENST00000525849.5:c.1556G>A (EYA4)	ENSP00000433219.1:p.Cys519Tyr
ENST00000525849.6:c.1556G>A (EYA4)	ENSP00000433219.1:p.Cys519Tyr
ENST00000525849.7:c.1556G>A (EYA4)	ENSP00000433219.1:p.Cys519Tyr
ENST00000531901.5:c.1643G>A (EYA4)	ENSP00000432770.1:p.Cys548Tyr
ENST00000683325.1:c.*198G>A (EYA4)	ENSP00000508141.1:n.*198G>A
ENST00000683674.1:n.526G>A (EYA4)
ENST00000684773.1:c.1148G>A (EYA4)	ENSP00000506812.1:p.Cys383Tyr
ENST00000706301.1:c.1463G>A (EYA4)	ENSP00000516341.1:p.Cys488Tyr
XM_005266851.3:c.1643G>A (EYA4)	XP_005266908.1:p.Cys548Tyr
XM_005266851.5:c.1643G>A (EYA4)	XP_005266908.1:p.Cys548Tyr
XM_005266852.3:c.1643G>A (EYA4)	XP_005266909.1:p.Cys548Tyr
XM_005266853.3:c.1556G>A (EYA4)	XP_005266910.1:p.Cys519Tyr
XM_005266853.5:c.1556G>A (EYA4)	XP_005266910.1:p.Cys519Tyr
XM_011535540.1:c.1574G>A (EYA4)	XP_011533842.1:p.Cys525Tyr
XM_011535541.1:c.1559G>A (EYA4)	XP_011533843.1:p.Cys520Tyr
XM_011535542.1:c.1481G>A (EYA4)	XP_011533844.1:p.Cys494Tyr
XM_017010368.2:c.1643G>A (EYA4)	XP_016865857.1:p.Cys548Tyr
XM_017010369.2:c.1625G>A (EYA4)	XP_016865858.1:p.Cys542Tyr
XM_017010370.2:c.1574G>A (EYA4)	XP_016865859.1:p.Cys525Tyr
XM_017010371.2:c.1559G>A (EYA4)	XP_016865860.1:p.Cys520Tyr
XM_017010372.2:c.1481G>A (EYA4)	XP_016865861.1:p.Cys494Tyr
XM_017010373.2:c.1463G>A (EYA4)	XP_016865862.1:p.Cys488Tyr
XM_017010374.2:c.1481G>A (EYA4)	XP_016865863.1:p.Cys494Tyr
XM_017010375.1:c.1481G>A (EYA4)	XP_016865864.1:p.Cys494Tyr
XR_001743220.2:n.1719G>A (EYA4)