Canonical Allele Identifier: CA4008521

Gene: EYA4 TARID

Linked Data

• dbSNP Id: rs762378482
• ExAC: 6:133849967 AT / A
• gnomAD v2: 6-133849967-AT-A
• gnomAD v4: 6-133528829-AT-A
• MyVariant Identifiers: chr6:g.133849968del (hg19) ; chr6:g.133528830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133528835del , CM000668.2:g.133528835del	GRCh38
NC_000006.11:g.133849973del , CM000668.1:g.133849973del	GRCh37
NC_000006.10:g.133891666del	NCBI36
NG_011596.1:g.292479del
NG_011596.2:g.292479del

Transcript Alleles

HGVS	Amino-acid change
ENST00000525849.7:c.*30del (EYA4)	ENSP00000433219.1:n.*30del
ENST00000706301.1:c.*30del (EYA4)	ENSP00000516341.1:n.*30del
ENST00000355167.8:c.*30del (EYA4)	ENSP00000347294.4:n.*30del
ENST00000683325.1:c.*4132del (EYA4)	ENSP00000508141.1:n.*4132del
ENST00000355286.12:c.*30del (EYA4) MANE Select	ENSP00000347434.7:n.*30del
ENST00000431403.3:c.*30del (EYA4)	ENSP00000404558.3:n.*30del
ENST00000525849.6:c.*30del (EYA4)	ENSP00000433219.1:n.*30del
ENST00000355167.7:c.*30del (EYA4)	ENSP00000347294.3:n.*30del
ENST00000355286.10:c.*30del (EYA4)	ENSP00000347434.6:n.*30del
ENST00000367895.9:c.*30del (EYA4)	ENSP00000356870.5:n.*30del
ENST00000430974.6:c.1696-2374del (EYA4)	ENSP00000388670.2:n.1696-2374del
ENST00000431403.2:c.1950del (EYA4)	ENSP00000404558.2:n.1950del
ENST00000452339.6:c.*30del (EYA4)	ENSP00000395916.2:n.*30del
ENST00000525849.5:c.*30del (EYA4)	ENSP00000433219.1:n.*30del
ENST00000531901.5:c.*30del (EYA4)	ENSP00000432770.1:n.*30del
NM_001301012.1:c.*30del (EYA4)	NP_001287941.1:n.*30del
NM_001301013.1:c.*30del (EYA4)	NP_001287942.1:n.*30del
NM_004100.4:c.*30del (EYA4)	NP_004091.3:n.*30del
NM_172103.3:c.*30del (EYA4)	NP_742101.2:n.*30del
NM_172105.3:c.*30del (EYA4)	NP_742103.1:n.*30del
NR_109982.1:n.2285+6950del (TARID)
XM_005266851.3:c.*30del (EYA4)	XP_005266908.1:n.*30del
XM_005266853.3:c.*30del (EYA4)	XP_005266910.1:n.*30del
XM_011535540.1:c.1900del (EYA4)	XP_011533842.1:p.Tyr634IlefsTer6
XM_011535541.1:c.1885del (EYA4)	XP_011533843.1:p.Tyr629IlefsTer6
XM_011535542.1:c.1807del (EYA4)	XP_011533844.1:p.Tyr603IlefsTer6
XM_005266851.5:c.*30del (EYA4)	XP_005266908.1:n.*30del
XM_005266853.5:c.*30del (EYA4)	XP_005266910.1:n.*30del
XM_017010368.2:c.*3473del (EYA4)	XP_016865857.1:n.*3473del
XM_017010369.2:c.*3473del (EYA4)	XP_016865858.1:n.*3473del
XM_017010370.2:c.*3473del (EYA4)	XP_016865859.1:n.*3473del
XM_017010371.2:c.*3473del (EYA4)	XP_016865860.1:n.*3473del
XM_017010372.2:c.*3473del (EYA4)	XP_016865861.1:n.*3473del
XM_017010373.2:c.*3473del (EYA4)	XP_016865862.1:n.*3473del
XM_017010374.2:c.*30del (EYA4)	XP_016865863.1:n.*30del
XM_017010375.1:c.*30del (EYA4)	XP_016865864.1:n.*30del
XR_001743220.2:n.5653del (EYA4)
NM_004100.5:c.*30del (EYA4) MANE Select	NP_004091.3:n.*30del
NM_001370458.1:c.*30del (EYA4)	NP_001357387.1:n.*30del
NM_001370459.1:c.*30del (EYA4)	NP_001357388.1:n.*30del
NM_001301012.2:c.*30del (EYA4)	NP_001287941.1:n.*30del
NM_001301013.2:c.*30del (EYA4)	NP_001287942.1:n.*30del
NM_172103.4:c.*30del (EYA4)	NP_742101.2:n.*30del
NM_172105.4:c.*30del (EYA4)	NP_742103.1:n.*30del