Canonical Allele Identifier: CA371466839
Gene: EYA1 HGNC NCBI

Linked Data

dbSNP Id: rs1392799354
gnomAD v2: 8-72129056-C-G
gnomAD v3: 8-71216821-C-G
gnomAD v4: 8-71216821-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.71216821C>G , CM000670.2:g.71216821C>G GRCh38
NC_000008.10:g.72129056C>G , CM000670.1:g.72129056C>G GRCh37
NC_000008.9:g.72291610C>G NCBI36
NG_011735.2:g.150412G>C
NG_011735.3:g.336310G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000340726.8:c.1231G>C MANE Select ENSP00000342626.3:p.Ala411Pro
ENST00000388741.7:c.1129G>C ENSP00000373393.2:p.Ala377Pro
ENST00000419131.6:c.1126G>C ENSP00000410176.1:p.Ala376Pro
ENST00000465115.6:c.*510G>C ENSP00000428391.1:n.*510G>C
ENST00000493349.2:c.621G>C
ENST00000496494.6:n.1694G>C
ENST00000642391.1:c.*908G>C ENSP00000496700.1:n.*908G>C
ENST00000643681.1:c.1318G>C ENSP00000495390.1:p.Ala440Pro
ENST00000644229.1:c.1213G>C ENSP00000494568.1:p.Ala405Pro
ENST00000644424.1:n.301G>C
ENST00000644712.1:c.1210G>C ENSP00000496188.1:p.Ala404Pro
ENST00000645793.1:c.1231G>C ENSP00000496255.1:p.Ala411Pro
ENST00000647540.1:c.1231G>C ENSP00000494438.1:p.Ala411Pro
ENST00000303824.11:c.1213G>C ENSP00000303221.7:p.Ala405Pro
ENST00000340726.7:c.1231G>C ENSP00000342626.3:p.Ala411Pro
ENST00000388740.4:c.1132G>C ENSP00000373392.3:p.Ala378Pro
ENST00000388741.6:c.1129G>C ENSP00000373393.2:p.Ala377Pro
ENST00000388742.8:c.1231G>C ENSP00000373394.4:p.Ala411Pro
ENST00000388743.6:c.1228G>C ENSP00000373395.2:p.Ala410Pro
ENST00000419131.5:c.1126G>C ENSP00000410176.1:p.Ala376Pro
ENST00000465115.5:c.*510G>C ENSP00000428391.1:n.*510G>C
ENST00000493349.1:c.*176G>C ENSP00000428517.1:n.*176G>C
ENST00000496494.5:n.1726G>C
NM_000503.5:c.1231G>C NP_000494.2:p.Ala411Pro
NM_001288574.1:c.1213G>C NP_001275503.1:p.Ala405Pro
NM_001288575.1:c.865G>C NP_001275504.1:p.Ala289Pro
NM_172058.3:c.1231G>C NP_742055.1:p.Ala411Pro
NM_172059.3:c.1126G>C NP_742056.1:p.Ala376Pro
NM_172060.3:c.1132G>C NP_742057.1:p.Ala378Pro
XM_011517481.1:c.1303G>C XP_011515783.1:p.Ala435Pro
XM_011517482.1:c.1318G>C XP_011515784.1:p.Ala440Pro
XM_011517483.1:c.1228G>C XP_011515785.1:p.Ala410Pro
XM_011517484.1:c.1216G>C XP_011515786.1:p.Ala406Pro
XM_011517485.1:c.1231G>C XP_011515787.1:p.Ala411Pro
XM_011517486.1:c.1231G>C XP_011515788.1:p.Ala411Pro
XM_011517487.1:c.1231G>C XP_011515789.1:p.Ala411Pro
XM_011517488.1:c.1228G>C XP_011515790.1:p.Ala410Pro
XM_011517489.1:c.1168G>C XP_011515791.1:p.Ala390Pro
XM_011517490.1:c.1132G>C XP_011515792.1:p.Ala378Pro
XM_011517491.1:c.1132G>C XP_011515793.1:p.Ala378Pro
XM_011517492.1:c.880G>C XP_011515794.1:p.Ala294Pro
NM_172059.4:c.1213G>C NP_742056.2:p.Ala405Pro
XM_011517483.2:c.1228G>C XP_011515785.1:p.Ala410Pro
XM_011517484.3:c.1303G>C XP_011515786.2:p.Ala435Pro
XM_017013201.1:c.1318G>C XP_016868690.1:p.Ala440Pro
XM_017013202.1:c.1318G>C XP_016868691.1:p.Ala440Pro
XM_017013203.2:c.1315G>C XP_016868692.1:p.Ala439Pro
XM_017013204.2:c.1300G>C XP_016868693.1:p.Ala434Pro
XM_017013205.2:c.1318G>C XP_016868694.1:p.Ala440Pro
XM_017013206.1:c.1231G>C XP_016868695.1:p.Ala411Pro
XM_017013207.2:c.1228G>C XP_016868696.1:p.Ala410Pro
XM_017013208.2:c.1228G>C XP_016868697.1:p.Ala410Pro
XM_017013210.2:c.1210G>C XP_016868699.1:p.Ala404Pro
XM_017013211.2:c.1168G>C XP_016868700.1:p.Ala390Pro
XM_017013212.2:c.1132G>C XP_016868701.1:p.Ala378Pro
XM_017013213.1:c.880G>C XP_016868702.1:p.Ala294Pro
NM_000503.6:c.1231G>C MANE Select NP_000494.2:p.Ala411Pro
NM_001288574.2:c.1213G>C NP_001275503.1:p.Ala405Pro
NM_001288575.2:c.865G>C NP_001275504.1:p.Ala289Pro
NM_001370333.1:c.1318G>C NP_001357262.1:p.Ala440Pro
NM_001370334.1:c.1231G>C NP_001357263.1:p.Ala411Pro
NM_001370335.1:c.1231G>C NP_001357264.1:p.Ala411Pro
NM_001370336.1:c.1210G>C NP_001357265.1:p.Ala404Pro
NM_172058.4:c.1231G>C NP_742055.1:p.Ala411Pro
NM_172059.5:c.1213G>C NP_742056.2:p.Ala405Pro