Canonical Allele Identifier: CA1792716258
Gene: EYA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.71271844G= , CM000670.2:g.71271844G= GRCh38
NC_000008.10:g.72184079G= , CM000670.1:g.72184079G= GRCh37
NC_000008.9:g.72346633G= NCBI36
NG_011735.2:g.95389C=
NG_011735.3:g.281287C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340726.8:c.880C= MANE Select ENSP00000342626.3:p.Arg294=
ENST00000388741.7:c.778C= ENSP00000373393.2:p.Arg260=
ENST00000419131.6:c.865C= ENSP00000410176.1:p.Arg289=
ENST00000465115.6:c.*159C= ENSP00000428391.1:n.*159C=
ENST00000493349.2:c.116C=
ENST00000496494.6:n.1343C=
ENST00000642391.1:c.*647C= ENSP00000496700.1:n.*647C=
ENST00000643681.1:c.967C= ENSP00000495390.1:p.Arg323=
ENST00000644229.1:c.952C= ENSP00000494568.1:p.Arg318=
ENST00000644712.1:c.949C= ENSP00000496188.1:p.Arg317=
ENST00000645793.1:c.880C= ENSP00000496255.1:p.Arg294=
ENST00000647540.1:c.880C= ENSP00000494438.1:p.Arg294=
ENST00000303824.11:c.862C= ENSP00000303221.7:p.Arg288=
ENST00000340726.7:c.880C= ENSP00000342626.3:p.Arg294=
ENST00000388740.4:c.781C= ENSP00000373392.3:p.Arg261=
ENST00000388741.6:c.778C= ENSP00000373393.2:p.Arg260=
ENST00000388742.8:c.880C= ENSP00000373394.4:p.Arg294=
ENST00000388743.6:c.877C= ENSP00000373395.2:p.Arg293=
ENST00000419131.5:c.865C= ENSP00000410176.1:p.Arg289=
ENST00000465115.5:c.*159C= ENSP00000428391.1:n.*159C=
ENST00000493349.1:c.-204C= ENSP00000428517.1:n.-204C=
ENST00000496494.5:n.1375C=
NM_000503.5:c.880C= NP_000494.2:p.Arg294=
NM_001288574.1:c.862C= NP_001275503.1:p.Arg288=
NM_001288575.1:c.514C= NP_001275504.1:p.Arg172=
NM_172058.3:c.880C= NP_742055.1:p.Arg294=
NM_172059.3:c.865C= NP_742056.1:p.Arg289=
NM_172060.3:c.781C= NP_742057.1:p.Arg261=
XM_011517481.1:c.952C= XP_011515783.1:p.Arg318=
XM_011517482.1:c.967C= XP_011515784.1:p.Arg323=
XM_011517483.1:c.877C= XP_011515785.1:p.Arg293=
XM_011517484.1:c.865C= XP_011515786.1:p.Arg289=
XM_011517485.1:c.880C= XP_011515787.1:p.Arg294=
XM_011517486.1:c.880C= XP_011515788.1:p.Arg294=
XM_011517487.1:c.880C= XP_011515789.1:p.Arg294=
XM_011517488.1:c.877C= XP_011515790.1:p.Arg293=
XM_011517489.1:c.817C= XP_011515791.1:p.Arg273=
XM_011517490.1:c.781C= XP_011515792.1:p.Arg261=
XM_011517491.1:c.781C= XP_011515793.1:p.Arg261=
XM_011517492.1:c.529C= XP_011515794.1:p.Arg177=
NM_172059.4:c.952C= NP_742056.2:p.Arg318=
XM_011517483.2:c.877C= XP_011515785.1:p.Arg293=
XM_011517484.3:c.952C= XP_011515786.2:p.Arg318=
XM_017013201.1:c.967C= XP_016868690.1:p.Arg323=
XM_017013202.1:c.967C= XP_016868691.1:p.Arg323=
XM_017013203.2:c.964C= XP_016868692.1:p.Arg322=
XM_017013204.2:c.949C= XP_016868693.1:p.Arg317=
XM_017013205.2:c.967C= XP_016868694.1:p.Arg323=
XM_017013206.1:c.880C= XP_016868695.1:p.Arg294=
XM_017013207.2:c.967C= XP_016868696.1:p.Arg323=
XM_017013208.2:c.877C= XP_016868697.1:p.Arg293=
XM_017013210.2:c.949C= XP_016868699.1:p.Arg317=
XM_017013211.2:c.817C= XP_016868700.1:p.Arg273=
XM_017013212.2:c.781C= XP_016868701.1:p.Arg261=
XM_017013213.1:c.529C= XP_016868702.1:p.Arg177=
NM_000503.6:c.880C= MANE Select NP_000494.2:p.Arg294=
NM_001288574.2:c.862C= NP_001275503.1:p.Arg288=
NM_001288575.2:c.514C= NP_001275504.1:p.Arg172=
NM_001370333.1:c.967C= NP_001357262.1:p.Arg323=
NM_001370334.1:c.880C= NP_001357263.1:p.Arg294=
NM_001370335.1:c.880C= NP_001357264.1:p.Arg294=
NM_001370336.1:c.949C= NP_001357265.1:p.Arg317=
NM_172058.4:c.880C= NP_742055.1:p.Arg294=
NM_172059.5:c.952C= NP_742056.2:p.Arg318=