Canonical Allele Identifier: CA1792716252

Gene: EYA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.71271835G= , CM000670.2:g.71271835G=	GRCh38
NC_000008.10:g.72184070G= , CM000670.1:g.72184070G=	GRCh37
NC_000008.9:g.72346624G=	NCBI36
NG_011735.2:g.95398C=
NG_011735.3:g.281296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340726.8:c.889C= MANE Select	ENSP00000342626.3:p.Arg297=
ENST00000388741.7:c.787C=	ENSP00000373393.2:p.Arg263=
ENST00000419131.6:c.874C=	ENSP00000410176.1:p.Arg292=
ENST00000465115.6:c.*168C=	ENSP00000428391.1:n.*168C=
ENST00000493349.2:c.125C=
ENST00000496494.6:n.1352C=
ENST00000642391.1:c.*656C=	ENSP00000496700.1:n.*656C=
ENST00000643681.1:c.976C=	ENSP00000495390.1:p.Arg326=
ENST00000644229.1:c.961C=	ENSP00000494568.1:p.Arg321=
ENST00000644712.1:c.958C=	ENSP00000496188.1:p.Arg320=
ENST00000645793.1:c.889C=	ENSP00000496255.1:p.Arg297=
ENST00000647540.1:c.889C=	ENSP00000494438.1:p.Arg297=
ENST00000303824.11:c.871C=	ENSP00000303221.7:p.Arg291=
ENST00000340726.7:c.889C=	ENSP00000342626.3:p.Arg297=
ENST00000388740.4:c.790C=	ENSP00000373392.3:p.Arg264=
ENST00000388741.6:c.787C=	ENSP00000373393.2:p.Arg263=
ENST00000388742.8:c.889C=	ENSP00000373394.4:p.Arg297=
ENST00000388743.6:c.886C=	ENSP00000373395.2:p.Arg296=
ENST00000419131.5:c.874C=	ENSP00000410176.1:p.Arg292=
ENST00000465115.5:c.*168C=	ENSP00000428391.1:n.*168C=
ENST00000493349.1:c.-195C=	ENSP00000428517.1:n.-195C=
ENST00000496494.5:n.1384C=
NM_000503.5:c.889C=	NP_000494.2:p.Arg297=
NM_001288574.1:c.871C=	NP_001275503.1:p.Arg291=
NM_001288575.1:c.523C=	NP_001275504.1:p.Arg175=
NM_172058.3:c.889C=	NP_742055.1:p.Arg297=
NM_172059.3:c.874C=	NP_742056.1:p.Arg292=
NM_172060.3:c.790C=	NP_742057.1:p.Arg264=
XM_011517481.1:c.961C=	XP_011515783.1:p.Arg321=
XM_011517482.1:c.976C=	XP_011515784.1:p.Arg326=
XM_011517483.1:c.886C=	XP_011515785.1:p.Arg296=
XM_011517484.1:c.874C=	XP_011515786.1:p.Arg292=
XM_011517485.1:c.889C=	XP_011515787.1:p.Arg297=
XM_011517486.1:c.889C=	XP_011515788.1:p.Arg297=
XM_011517487.1:c.889C=	XP_011515789.1:p.Arg297=
XM_011517488.1:c.886C=	XP_011515790.1:p.Arg296=
XM_011517489.1:c.826C=	XP_011515791.1:p.Arg276=
XM_011517490.1:c.790C=	XP_011515792.1:p.Arg264=
XM_011517491.1:c.790C=	XP_011515793.1:p.Arg264=
XM_011517492.1:c.538C=	XP_011515794.1:p.Arg180=
NM_172059.4:c.961C=	NP_742056.2:p.Arg321=
XM_011517483.2:c.886C=	XP_011515785.1:p.Arg296=
XM_011517484.3:c.961C=	XP_011515786.2:p.Arg321=
XM_017013201.1:c.976C=	XP_016868690.1:p.Arg326=
XM_017013202.1:c.976C=	XP_016868691.1:p.Arg326=
XM_017013203.2:c.973C=	XP_016868692.1:p.Arg325=
XM_017013204.2:c.958C=	XP_016868693.1:p.Arg320=
XM_017013205.2:c.976C=	XP_016868694.1:p.Arg326=
XM_017013206.1:c.889C=	XP_016868695.1:p.Arg297=
XM_017013207.2:c.976C=	XP_016868696.1:p.Arg326=
XM_017013208.2:c.886C=	XP_016868697.1:p.Arg296=
XM_017013210.2:c.958C=	XP_016868699.1:p.Arg320=
XM_017013211.2:c.826C=	XP_016868700.1:p.Arg276=
XM_017013212.2:c.790C=	XP_016868701.1:p.Arg264=
XM_017013213.1:c.538C=	XP_016868702.1:p.Arg180=
NM_000503.6:c.889C= MANE Select	NP_000494.2:p.Arg297=
NM_001288574.2:c.871C=	NP_001275503.1:p.Arg291=
NM_001288575.2:c.523C=	NP_001275504.1:p.Arg175=
NM_001370333.1:c.976C=	NP_001357262.1:p.Arg326=
NM_001370334.1:c.889C=	NP_001357263.1:p.Arg297=
NM_001370335.1:c.889C=	NP_001357264.1:p.Arg297=
NM_001370336.1:c.958C=	NP_001357265.1:p.Arg320=
NM_172058.4:c.889C=	NP_742055.1:p.Arg297=
NM_172059.5:c.961C=	NP_742056.2:p.Arg321=