Canonical Allele Identifier: CA2503107901
Gene: EYA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.71216733_71216734insAAAATC , CM000670.2:g.71216733_71216734insAAAATC GRCh38
NC_000008.10:g.72128968_72128969insAAAATC , CM000670.1:g.72128968_72128969insAAAATC GRCh37
NC_000008.9:g.72291522_72291523insAAAATC NCBI36
NG_011735.2:g.150500_150501insATTTTG
NG_011735.3:g.336398_336399insATTTTG

Transcript Alleles

HGVS Amino-acid change
ENST00000340726.8:c.1319_1320insATTTTG MANE Select ENSP00000342626.3:p.Arg440_Val441insPheTr...
ENST00000388741.7:c.1217_1218insATTTTG ENSP00000373393.2:p.Arg406_Val407insPheTr...
ENST00000419131.6:c.1214_1215insATTTTG ENSP00000410176.1:p.Arg405_Val406insPheTr...
ENST00000465115.6:c.*598_*599insATTTTG ENSP00000428391.1:n.*598_*599insATTTTG
ENST00000493349.2:c.709_710insATTTTG
ENST00000496494.6:n.1782_1783insATTTTG
ENST00000642391.1:c.*996_*997insATTTTG ENSP00000496700.1:n.*996_*997insATTTTG
ENST00000643681.1:c.1406_1407insATTTTG ENSP00000495390.1:p.Arg469_Val470insPheTr...
ENST00000644229.1:c.1301_1302insATTTTG ENSP00000494568.1:p.Arg434_Val435insPheTr...
ENST00000644424.1:n.389_390insATTTTG
ENST00000644712.1:c.1298_1299insATTTTG ENSP00000496188.1:p.Arg433_Val434insPheTr...
ENST00000645793.1:c.1319_1320insATTTTG ENSP00000496255.1:p.Arg440_Val441insPheTr...
ENST00000647540.1:c.1319_1320insATTTTG ENSP00000494438.1:p.Arg440_Val441insPheTr...
ENST00000303824.11:c.1301_1302insATTTTG ENSP00000303221.7:p.Arg434_Val435insPheTr...
ENST00000340726.7:c.1319_1320insATTTTG ENSP00000342626.3:p.Arg440_Val441insPheTr...
ENST00000388740.4:c.1220_1221insATTTTG ENSP00000373392.3:p.Arg407_Val408insPheTr...
ENST00000388741.6:c.1217_1218insATTTTG ENSP00000373393.2:p.Arg406_Val407insPheTr...
ENST00000388742.8:c.1319_1320insATTTTG ENSP00000373394.4:p.Arg440_Val441insPheTr...
ENST00000388743.6:c.1316_1317insATTTTG ENSP00000373395.2:p.Arg439_Val440insPheTr...
ENST00000419131.5:c.1214_1215insATTTTG ENSP00000410176.1:p.Arg405_Val406insPheTr...
ENST00000465115.5:c.*598_*599insATTTTG ENSP00000428391.1:n.*598_*599insATTTTG
ENST00000493349.1:c.*264_*265insATTTTG ENSP00000428517.1:n.*264_*265insATTTTG
ENST00000496494.5:n.1814_1815insATTTTG
NM_000503.5:c.1319_1320insATTTTG NP_000494.2:p.Arg440_Val441insPheTrp
NM_001288574.1:c.1301_1302insATTTTG NP_001275503.1:p.Arg434_Val435insPheTrp
NM_001288575.1:c.953_954insATTTTG NP_001275504.1:p.Arg318_Val319insPheTrp
NM_172058.3:c.1319_1320insATTTTG NP_742055.1:p.Arg440_Val441insPheTrp
NM_172059.3:c.1214_1215insATTTTG NP_742056.1:p.Arg405_Val406insPheTrp
NM_172060.3:c.1220_1221insATTTTG NP_742057.1:p.Arg407_Val408insPheTrp
XM_011517481.1:c.1391_1392insATTTTG XP_011515783.1:p.Arg464_Val465insPheTrp
XM_011517482.1:c.1406_1407insATTTTG XP_011515784.1:p.Arg469_Val470insPheTrp
XM_011517483.1:c.1316_1317insATTTTG XP_011515785.1:p.Arg439_Val440insPheTrp
XM_011517484.1:c.1304_1305insATTTTG XP_011515786.1:p.Arg435_Val436insPheTrp
XM_011517485.1:c.1319_1320insATTTTG XP_011515787.1:p.Arg440_Val441insPheTrp
XM_011517486.1:c.1319_1320insATTTTG XP_011515788.1:p.Arg440_Val441insPheTrp
XM_011517487.1:c.1319_1320insATTTTG XP_011515789.1:p.Arg440_Val441insPheTrp
XM_011517488.1:c.1316_1317insATTTTG XP_011515790.1:p.Arg439_Val440insPheTrp
XM_011517489.1:c.1256_1257insATTTTG XP_011515791.1:p.Arg419_Val420insPheTrp
XM_011517490.1:c.1220_1221insATTTTG XP_011515792.1:p.Arg407_Val408insPheTrp
XM_011517491.1:c.1220_1221insATTTTG XP_011515793.1:p.Arg407_Val408insPheTrp
XM_011517492.1:c.968_969insATTTTG XP_011515794.1:p.Arg323_Val324insPheTrp
NM_172059.4:c.1301_1302insATTTTG NP_742056.2:p.Arg434_Val435insPheTrp
XM_011517483.2:c.1316_1317insATTTTG XP_011515785.1:p.Arg439_Val440insPheTrp
XM_011517484.3:c.1391_1392insATTTTG XP_011515786.2:p.Arg464_Val465insPheTrp
XM_017013201.1:c.1406_1407insATTTTG XP_016868690.1:p.Arg469_Val470insPheTrp
XM_017013202.1:c.1406_1407insATTTTG XP_016868691.1:p.Arg469_Val470insPheTrp
XM_017013203.2:c.1403_1404insATTTTG XP_016868692.1:p.Arg468_Val469insPheTrp
XM_017013204.2:c.1388_1389insATTTTG XP_016868693.1:p.Arg463_Val464insPheTrp
XM_017013205.2:c.1406_1407insATTTTG XP_016868694.1:p.Arg469_Val470insPheTrp
XM_017013206.1:c.1319_1320insATTTTG XP_016868695.1:p.Arg440_Val441insPheTrp
XM_017013207.2:c.1316_1317insATTTTG XP_016868696.1:p.Arg439_Val440insPheTrp
XM_017013208.2:c.1316_1317insATTTTG XP_016868697.1:p.Arg439_Val440insPheTrp
XM_017013210.2:c.1298_1299insATTTTG XP_016868699.1:p.Arg433_Val434insPheTrp
XM_017013211.2:c.1256_1257insATTTTG XP_016868700.1:p.Arg419_Val420insPheTrp
XM_017013212.2:c.1220_1221insATTTTG XP_016868701.1:p.Arg407_Val408insPheTrp
XM_017013213.1:c.968_969insATTTTG XP_016868702.1:p.Arg323_Val324insPheTrp
NM_000503.6:c.1319_1320insATTTTG MANE Select NP_000494.2:p.Arg440_Val441insPheTrp
NM_001288574.2:c.1301_1302insATTTTG NP_001275503.1:p.Arg434_Val435insPheTrp
NM_001288575.2:c.953_954insATTTTG NP_001275504.1:p.Arg318_Val319insPheTrp
NM_001370333.1:c.1406_1407insATTTTG NP_001357262.1:p.Arg469_Val470insPheTrp
NM_001370334.1:c.1319_1320insATTTTG NP_001357263.1:p.Arg440_Val441insPheTrp
NM_001370335.1:c.1319_1320insATTTTG NP_001357264.1:p.Arg440_Val441insPheTrp
NM_001370336.1:c.1298_1299insATTTTG NP_001357265.1:p.Arg433_Val434insPheTrp
NM_172058.4:c.1319_1320insATTTTG NP_742055.1:p.Arg440_Val441insPheTrp
NM_172059.5:c.1301_1302insATTTTG NP_742056.2:p.Arg434_Val435insPheTrp