Canonical Allele Identifier: CA1665002117

Gene: EYA4

Linked Data

• dbSNP Id: rs1554261974

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133462475_133462476insGGGA , CM000668.2:g.133462475_133462476insGGGA	GRCh38
NC_000006.11:g.133783613_133783614insGGGA , CM000668.1:g.133783613_133783614insGGGA	GRCh37
NC_000006.10:g.133825306_133825307insGGGA	NCBI36
NG_011596.1:g.226119_226120insGGGA
NG_011596.2:g.226119_226120insGGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525849.7:c.509_510insGGGA	ENSP00000433219.1:p.Tyr170Ter
ENST00000706301.1:c.416_417insGGGA	ENSP00000516341.1:p.Tyr139Ter
ENST00000355167.8:c.416_417insGGGA	ENSP00000347294.4:p.Tyr139Ter
ENST00000497350.3:n.666_667insGGGA
ENST00000683325.1:c.101_102insGGGA	ENSP00000508141.1:p.Tyr34Ter
ENST00000683664.1:n.544_545insGGGA
ENST00000684773.1:c.101_102insGGGA	ENSP00000506812.1:p.Tyr34Ter
ENST00000355286.12:c.578_579insGGGA MANE Select	ENSP00000347434.7:p.Tyr193Ter
ENST00000431403.3:c.509_510insGGGA	ENSP00000404558.3:p.Tyr170Ter
ENST00000525849.6:c.509_510insGGGA	ENSP00000433219.1:p.Tyr170Ter
ENST00000355167.7:c.578_579insGGGA	ENSP00000347294.3:p.Tyr193Ter
ENST00000355286.10:c.509_510insGGGA	ENSP00000347434.6:p.Tyr170Ter
ENST00000367895.9:c.578_579insGGGA	ENSP00000356870.5:p.Tyr193Ter
ENST00000421413.6:n.651_652insGGGA
ENST00000430974.6:c.416_417insGGGA	ENSP00000388670.2:p.Tyr139Ter
ENST00000431403.2:c.578_579insGGGA	ENSP00000404558.2:p.Tyr193Ter
ENST00000452339.6:c.416_417insGGGA	ENSP00000395916.2:p.Tyr139Ter
ENST00000497350.2:n.355_356insGGGA
ENST00000525849.5:c.509_510insGGGA	ENSP00000433219.1:p.Tyr170Ter
ENST00000531861.5:n.578_579insGGGA
ENST00000531901.5:c.578_579insGGGA	ENSP00000432770.1:p.Tyr193Ter
NM_001301012.1:c.416_417insGGGA	NP_001287941.1:p.Tyr139Ter
NM_001301013.1:c.578_579insGGGA	NP_001287942.1:p.Tyr193Ter
NM_004100.4:c.578_579insGGGA	NP_004091.3:p.Tyr193Ter
NM_172103.3:c.509_510insGGGA	NP_742101.2:p.Tyr170Ter
NM_172105.3:c.578_579insGGGA	NP_742103.1:p.Tyr193Ter
XM_005266851.3:c.578_579insGGGA	XP_005266908.1:p.Tyr193Ter
XM_005266852.3:c.578_579insGGGA	XP_005266909.1:p.Tyr193Ter
XM_005266853.3:c.509_510insGGGA	XP_005266910.1:p.Tyr170Ter
XM_011535540.1:c.509_510insGGGA	XP_011533842.1:p.Tyr170Ter
XM_011535541.1:c.494_495insGGGA	XP_011533843.1:p.Tyr165Ter
XM_011535542.1:c.416_417insGGGA	XP_011533844.1:p.Tyr139Ter
XM_005266851.5:c.578_579insGGGA	XP_005266908.1:p.Tyr193Ter
XM_005266853.5:c.509_510insGGGA	XP_005266910.1:p.Tyr170Ter
XM_017010368.2:c.578_579insGGGA	XP_016865857.1:p.Tyr193Ter
XM_017010369.2:c.578_579insGGGA	XP_016865858.1:p.Tyr193Ter
XM_017010370.2:c.509_510insGGGA	XP_016865859.1:p.Tyr170Ter
XM_017010371.2:c.494_495insGGGA	XP_016865860.1:p.Tyr165Ter
XM_017010372.2:c.416_417insGGGA	XP_016865861.1:p.Tyr139Ter
XM_017010373.2:c.416_417insGGGA	XP_016865862.1:p.Tyr139Ter
XM_017010374.2:c.416_417insGGGA	XP_016865863.1:p.Tyr139Ter
XM_017010375.1:c.416_417insGGGA	XP_016865864.1:p.Tyr139Ter
XR_001743219.2:n.740_741insGGGA
XR_001743220.2:n.740_741insGGGA
NM_004100.5:c.578_579insGGGA MANE Select	NP_004091.3:p.Tyr193Ter
NM_001370458.1:c.509_510insGGGA	NP_001357387.1:p.Tyr170Ter
NM_001370459.1:c.416_417insGGGA	NP_001357388.1:p.Tyr139Ter
NM_001301012.2:c.416_417insGGGA	NP_001287941.1:p.Tyr139Ter
NM_001301013.2:c.578_579insGGGA	NP_001287942.1:p.Tyr193Ter
NM_172103.4:c.509_510insGGGA	NP_742101.2:p.Tyr170Ter
NM_172105.4:c.578_579insGGGA	NP_742103.1:p.Tyr193Ter