Canonical Allele Identifier: CA2579187136

Gene: EYA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.71362222_71362223insCCTTACC , CM000670.2:g.71362222_71362223insCCTTACC	GRCh38
NC_000008.10:g.72274457_72274458insCCTTACC , CM000670.1:g.72274457_72274458insCCTTACC	GRCh37
NC_000008.9:g.72437011_72437012insCCTTACC	NCBI36
NG_011735.2:g.5013_5014insAAGGGGT
NG_011735.3:g.190911_190912insAAGGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643681.1:c.34-5709_34-5708insAAGGGGT	ENSP00000495390.1:n.34-5709_34-5708insAAGGGGT
ENST00000644229.1:c.34-5709_34-5708insAAGGGGT	ENSP00000494568.1:n.34-5709_34-5708insAAGGGGT
ENST00000644712.1:c.34-5709_34-5708insAAGGGGT	ENSP00000496188.1:n.34-5709_34-5708insAAGGGGT
ENST00000645793.1:c.-54-5709_-54-5708insAAGGGGT	ENSP00000496255.1:n.-54-5709_-54-5708insAAGGGGT
ENST00000647540.1:c.-54-5709_-54-5708insAAGGGGT	ENSP00000494438.1:n.-54-5709_-54-5708insAAGGGGT
ENST00000340726.7:c.-628_-627insAAGGGGT	ENSP00000342626.3:n.-628_-627insAAGGGGT
NM_000503.5:c.-628_-627insAAGGGGT	NP_000494.2:n.-628_-627insAAGGGGT
NM_001288574.1:c.-628_-627insAAGGGGT	NP_001275503.1:n.-628_-627insAAGGGGT
NM_001288575.1:c.-912_-911insAAGGGGT	NP_001275504.1:n.-912_-911insAAGGGGT
XM_011517481.1:c.22-5709_22-5708insAAGGGGT	XP_011515783.1:n.22-5709_22-5708insAAGGGGT
XM_011517482.1:c.34-5709_34-5708insAAGGGGT	XP_011515784.1:n.34-5709_34-5708insAAGGGGT
XM_011517485.1:c.-54-5709_-54-5708insAAGGGGT	XP_011515787.1:n.-54-5709_-54-5708insAAGGGGT
XM_011517486.1:c.-54-5709_-54-5708insAAGGGGT	XP_011515788.1:n.-54-5709_-54-5708insAAGGGGT
XM_011517487.1:c.-54-5709_-54-5708insAAGGGGT	XP_011515789.1:n.-54-5709_-54-5708insAAGGGGT
XM_011517489.1:c.12-5709_12-5708insAAGGGGT	XP_011515791.1:n.12-5709_12-5708insAAGGGGT
XM_011517491.1:c.-25-5709_-25-5708insAAGGGGT	XP_011515793.1:n.-25-5709_-25-5708insAAGGGGT
NM_172059.4:c.34-5709_34-5708insAAGGGGT	NP_742056.2:n.34-5709_34-5708insAAGGGGT
XM_011517484.3:c.34-5709_34-5708insAAGGGGT	XP_011515786.2:n.34-5709_34-5708insAAGGGGT
XM_017013201.1:c.34-5709_34-5708insAAGGGGT	XP_016868690.1:n.34-5709_34-5708insAAGGGGT
XM_017013202.1:c.34-5709_34-5708insAAGGGGT	XP_016868691.1:n.34-5709_34-5708insAAGGGGT
XM_017013203.2:c.34-5709_34-5708insAAGGGGT	XP_016868692.1:n.34-5709_34-5708insAAGGGGT
XM_017013204.2:c.34-5709_34-5708insAAGGGGT	XP_016868693.1:n.34-5709_34-5708insAAGGGGT
XM_017013205.2:c.34-5709_34-5708insAAGGGGT	XP_016868694.1:n.34-5709_34-5708insAAGGGGT
XM_017013206.1:c.-54-5709_-54-5708insAAGGGGT	XP_016868695.1:n.-54-5709_-54-5708insAAGGGGT
XM_017013207.2:c.34-5709_34-5708insAAGGGGT	XP_016868696.1:n.34-5709_34-5708insAAGGGGT
XM_017013210.2:c.34-5709_34-5708insAAGGGGT	XP_016868699.1:n.34-5709_34-5708insAAGGGGT
XM_017013211.2:c.12-5709_12-5708insAAGGGGT	XP_016868700.1:n.12-5709_12-5708insAAGGGGT
XM_017013212.2:c.-599_-598insAAGGGGT	XP_016868701.1:n.-599_-598insAAGGGGT
NM_001370333.1:c.34-5709_34-5708insAAGGGGT	NP_001357262.1:n.34-5709_34-5708insAAGGGGT
NM_001370334.1:c.-54-5709_-54-5708insAAGGGGT	NP_001357263.1:n.-54-5709_-54-5708insAAGGGGT
NM_001370335.1:c.-54-5709_-54-5708insAAGGGGT	NP_001357264.1:n.-54-5709_-54-5708insAAGGGGT
NM_001370336.1:c.34-5709_34-5708insAAGGGGT	NP_001357265.1:n.34-5709_34-5708insAAGGGGT
NM_172059.5:c.34-5709_34-5708insAAGGGGT	NP_742056.2:n.34-5709_34-5708insAAGGGGT