Canonical Allele Identifier: CA1792691453
Gene: EYA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.71215379C= , CM000670.2:g.71215379C= GRCh38
NC_000008.10:g.72127614C= , CM000670.1:g.72127614C= GRCh37
NC_000008.9:g.72290168C= NCBI36
NG_011735.2:g.151854G=
NG_011735.3:g.337752G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340726.8:c.1597+8G= MANE Select ENSP00000342626.3:n.1597+8G=
ENST00000388741.7:c.1495+8G= ENSP00000373393.2:n.1495+8G=
ENST00000419131.6:c.1492+8G= ENSP00000410176.1:n.1492+8G=
ENST00000465115.6:c.*876+8G= ENSP00000428391.1:n.*876+8G=
ENST00000496494.6:n.2060+8G=
ENST00000642391.1:c.*1274+8G= ENSP00000496700.1:n.*1274+8G=
ENST00000643681.1:c.1684+8G= ENSP00000495390.1:n.1684+8G=
ENST00000644229.1:c.1579+8G= ENSP00000494568.1:n.1579+8G=
ENST00000644424.1:n.667+8G=
ENST00000644712.1:c.1576+8G= ENSP00000496188.1:n.1576+8G=
ENST00000645793.1:c.1597+8G= ENSP00000496255.1:n.1597+8G=
ENST00000647540.1:c.1597+8G= ENSP00000494438.1:n.1597+8G=
ENST00000303824.11:c.1579+8G= ENSP00000303221.7:n.1579+8G=
ENST00000340726.7:c.1597+8G= ENSP00000342626.3:n.1597+8G=
ENST00000388740.4:c.1498+8G= ENSP00000373392.3:n.1498+8G=
ENST00000388741.6:c.1495+8G= ENSP00000373393.2:n.1495+8G=
ENST00000388742.8:c.1597+8G= ENSP00000373394.4:n.1597+8G=
ENST00000388743.6:c.1594+8G= ENSP00000373395.2:n.1594+8G=
ENST00000419131.5:c.1492+8G= ENSP00000410176.1:n.1492+8G=
ENST00000465115.5:c.*876+8G= ENSP00000428391.1:n.*876+8G=
ENST00000496494.5:n.2092+8G=
NM_000503.5:c.1597+8G= NP_000494.2:n.1597+8G=
NM_001288574.1:c.1579+8G= NP_001275503.1:n.1579+8G=
NM_001288575.1:c.1231+8G= NP_001275504.1:n.1231+8G=
NM_172058.3:c.1597+8G= NP_742055.1:n.1597+8G=
NM_172059.3:c.1492+8G= NP_742056.1:n.1492+8G=
NM_172060.3:c.1498+8G= NP_742057.1:n.1498+8G=
XM_011517481.1:c.1669+8G= XP_011515783.1:n.1669+8G=
XM_011517482.1:c.1684+8G= XP_011515784.1:n.1684+8G=
XM_011517483.1:c.1594+8G= XP_011515785.1:n.1594+8G=
XM_011517484.1:c.1582+8G= XP_011515786.1:n.1582+8G=
XM_011517485.1:c.1597+8G= XP_011515787.1:n.1597+8G=
XM_011517486.1:c.1597+8G= XP_011515788.1:n.1597+8G=
XM_011517487.1:c.1597+8G= XP_011515789.1:n.1597+8G=
XM_011517488.1:c.1594+8G= XP_011515790.1:n.1594+8G=
XM_011517489.1:c.1534+8G= XP_011515791.1:n.1534+8G=
XM_011517490.1:c.1498+8G= XP_011515792.1:n.1498+8G=
XM_011517491.1:c.1498+8G= XP_011515793.1:n.1498+8G=
XM_011517492.1:c.1246+8G= XP_011515794.1:n.1246+8G=
NM_172059.4:c.1579+8G= NP_742056.2:n.1579+8G=
XM_011517483.2:c.1594+8G= XP_011515785.1:n.1594+8G=
XM_011517484.3:c.1669+8G= XP_011515786.2:n.1669+8G=
XM_017013201.1:c.1684+8G= XP_016868690.1:n.1684+8G=
XM_017013202.1:c.1684+8G= XP_016868691.1:n.1684+8G=
XM_017013203.2:c.1681+8G= XP_016868692.1:n.1681+8G=
XM_017013204.2:c.1666+8G= XP_016868693.1:n.1666+8G=
XM_017013205.2:c.1684+8G= XP_016868694.1:n.1684+8G=
XM_017013206.1:c.1597+8G= XP_016868695.1:n.1597+8G=
XM_017013207.2:c.1594+8G= XP_016868696.1:n.1594+8G=
XM_017013208.2:c.1594+8G= XP_016868697.1:n.1594+8G=
XM_017013210.2:c.1576+8G= XP_016868699.1:n.1576+8G=
XM_017013211.2:c.1534+8G= XP_016868700.1:n.1534+8G=
XM_017013212.2:c.1498+8G= XP_016868701.1:n.1498+8G=
XM_017013213.1:c.1246+8G= XP_016868702.1:n.1246+8G=
NM_000503.6:c.1597+8G= MANE Select NP_000494.2:n.1597+8G=
NM_001288574.2:c.1579+8G= NP_001275503.1:n.1579+8G=
NM_001288575.2:c.1231+8G= NP_001275504.1:n.1231+8G=
NM_001370333.1:c.1684+8G= NP_001357262.1:n.1684+8G=
NM_001370334.1:c.1597+8G= NP_001357263.1:n.1597+8G=
NM_001370335.1:c.1597+8G= NP_001357264.1:n.1597+8G=
NM_001370336.1:c.1576+8G= NP_001357265.1:n.1576+8G=
NM_172058.4:c.1597+8G= NP_742055.1:n.1597+8G=
NM_172059.5:c.1579+8G= NP_742056.2:n.1579+8G=