Canonical Allele Identifier: CA371466190
Gene: EYA1 HGNC NCBI
MyVariant.info:
Revel Score:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.71215453T>C , CM000670.2:g.71215453T>C GRCh38
NC_000008.10:g.72127688T>C , CM000670.1:g.72127688T>C GRCh37
NC_000008.9:g.72290242T>C NCBI36
NG_011735.2:g.151780A>G
NG_011735.3:g.337678A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000340726.8:c.1531A>G MANE Select ENSP00000342626.3:p.Lys511Glu
ENST00000388741.7:c.1429A>G ENSP00000373393.2:p.Lys477Glu
ENST00000419131.6:c.1426A>G ENSP00000410176.1:p.Lys476Glu
ENST00000465115.6:c.*810A>G ENSP00000428391.1:n.*810A>G
ENST00000496494.6:n.1994A>G
ENST00000642391.1:c.*1208A>G ENSP00000496700.1:n.*1208A>G
ENST00000643681.1:c.1618A>G ENSP00000495390.1:p.Lys540Glu
ENST00000644229.1:c.1513A>G ENSP00000494568.1:p.Lys505Glu
ENST00000644424.1:n.601A>G
ENST00000644712.1:c.1510A>G ENSP00000496188.1:p.Lys504Glu
ENST00000645793.1:c.1531A>G ENSP00000496255.1:p.Lys511Glu
ENST00000647540.1:c.1531A>G ENSP00000494438.1:p.Lys511Glu
ENST00000303824.11:c.1513A>G ENSP00000303221.7:p.Lys505Glu
ENST00000340726.7:c.1531A>G ENSP00000342626.3:p.Lys511Glu
ENST00000388740.4:c.1432A>G ENSP00000373392.3:p.Lys478Glu
ENST00000388741.6:c.1429A>G ENSP00000373393.2:p.Lys477Glu
ENST00000388742.8:c.1531A>G ENSP00000373394.4:p.Lys511Glu
ENST00000388743.6:c.1528A>G ENSP00000373395.2:p.Lys510Glu
ENST00000419131.5:c.1426A>G ENSP00000410176.1:p.Lys476Glu
ENST00000465115.5:c.*810A>G ENSP00000428391.1:n.*810A>G
ENST00000496494.5:n.2026A>G
NM_000503.5:c.1531A>G NP_000494.2:p.Lys511Glu
NM_001288574.1:c.1513A>G NP_001275503.1:p.Lys505Glu
NM_001288575.1:c.1165A>G NP_001275504.1:p.Lys389Glu
NM_172058.3:c.1531A>G NP_742055.1:p.Lys511Glu
NM_172059.3:c.1426A>G NP_742056.1:p.Lys476Glu
NM_172060.3:c.1432A>G NP_742057.1:p.Lys478Glu
XM_011517481.1:c.1603A>G XP_011515783.1:p.Lys535Glu
XM_011517482.1:c.1618A>G XP_011515784.1:p.Lys540Glu
XM_011517483.1:c.1528A>G XP_011515785.1:p.Lys510Glu
XM_011517484.1:c.1516A>G XP_011515786.1:p.Lys506Glu
XM_011517485.1:c.1531A>G XP_011515787.1:p.Lys511Glu
XM_011517486.1:c.1531A>G XP_011515788.1:p.Lys511Glu
XM_011517487.1:c.1531A>G XP_011515789.1:p.Lys511Glu
XM_011517488.1:c.1528A>G XP_011515790.1:p.Lys510Glu
XM_011517489.1:c.1468A>G XP_011515791.1:p.Lys490Glu
XM_011517490.1:c.1432A>G XP_011515792.1:p.Lys478Glu
XM_011517491.1:c.1432A>G XP_011515793.1:p.Lys478Glu
XM_011517492.1:c.1180A>G XP_011515794.1:p.Lys394Glu
NM_172059.4:c.1513A>G NP_742056.2:p.Lys505Glu
XM_011517483.2:c.1528A>G XP_011515785.1:p.Lys510Glu
XM_011517484.3:c.1603A>G XP_011515786.2:p.Lys535Glu
XM_017013201.1:c.1618A>G XP_016868690.1:p.Lys540Glu
XM_017013202.1:c.1618A>G XP_016868691.1:p.Lys540Glu
XM_017013203.2:c.1615A>G XP_016868692.1:p.Lys539Glu
XM_017013204.2:c.1600A>G XP_016868693.1:p.Lys534Glu
XM_017013205.2:c.1618A>G XP_016868694.1:p.Lys540Glu
XM_017013206.1:c.1531A>G XP_016868695.1:p.Lys511Glu
XM_017013207.2:c.1528A>G XP_016868696.1:p.Lys510Glu
XM_017013208.2:c.1528A>G XP_016868697.1:p.Lys510Glu
XM_017013210.2:c.1510A>G XP_016868699.1:p.Lys504Glu
XM_017013211.2:c.1468A>G XP_016868700.1:p.Lys490Glu
XM_017013212.2:c.1432A>G XP_016868701.1:p.Lys478Glu
XM_017013213.1:c.1180A>G XP_016868702.1:p.Lys394Glu
NM_000503.6:c.1531A>G MANE Select NP_000494.2:p.Lys511Glu
NM_001288574.2:c.1513A>G NP_001275503.1:p.Lys505Glu
NM_001288575.2:c.1165A>G NP_001275504.1:p.Lys389Glu
NM_001370333.1:c.1618A>G NP_001357262.1:p.Lys540Glu
NM_001370334.1:c.1531A>G NP_001357263.1:p.Lys511Glu
NM_001370335.1:c.1531A>G NP_001357264.1:p.Lys511Glu
NM_001370336.1:c.1510A>G NP_001357265.1:p.Lys504Glu
NM_172058.4:c.1531A>G NP_742055.1:p.Lys511Glu
NM_172059.5:c.1513A>G NP_742056.2:p.Lys505Glu