Canonical Allele Identifier: CA2780775328

Gene: EYA1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.71211074del , CM000670.2:g.71211074del	GRCh38
NC_000008.10:g.72123309del , CM000670.1:g.72123309del	GRCh37
NC_000008.9:g.72285863del	NCBI36
NG_011735.2:g.156160del
NG_011735.3:g.342058del

Transcript Alleles

HGVS	Amino-acid change
ENST00000340726.8:c.1698+83del MANE Select	ENSP00000342626.3:n.1698+83del
ENST00000388741.7:c.1596+83del	ENSP00000373393.2:n.1596+83del
ENST00000419131.6:c.1593+83del	ENSP00000410176.1:n.1593+83del
ENST00000465115.6:c.*977+83del	ENSP00000428391.1:n.*977+83del
ENST00000496494.6:n.2161+83del
ENST00000642391.1:c.*1375+83del	ENSP00000496700.1:n.*1375+83del
ENST00000643681.1:c.1785+83del	ENSP00000495390.1:n.1785+83del
ENST00000644229.1:c.1680+83del	ENSP00000494568.1:n.1680+83del
ENST00000644424.1:n.768+83del
ENST00000644712.1:c.1677+83del	ENSP00000496188.1:n.1677+83del
ENST00000645793.1:c.1698+83del	ENSP00000496255.1:n.1698+83del
ENST00000647540.1:c.1698+83del	ENSP00000494438.1:n.1698+83del
ENST00000303824.11:c.1680+83del	ENSP00000303221.7:n.1680+83del
ENST00000340726.7:c.1698+83del	ENSP00000342626.3:n.1698+83del
ENST00000388740.4:c.1599+83del	ENSP00000373392.3:n.1599+83del
ENST00000388741.6:c.1596+83del	ENSP00000373393.2:n.1596+83del
ENST00000388742.8:c.1698+83del	ENSP00000373394.4:n.1698+83del
ENST00000388743.6:c.1695+83del	ENSP00000373395.2:n.1695+83del
ENST00000419131.5:c.1593+83del	ENSP00000410176.1:n.1593+83del
ENST00000465115.5:c.*977+83del	ENSP00000428391.1:n.*977+83del
ENST00000496494.5:n.2193+83del
NM_000503.5:c.1698+83del	NP_000494.2:n.1698+83del
NM_001288574.1:c.1680+83del	NP_001275503.1:n.1680+83del
NM_001288575.1:c.1332+83del	NP_001275504.1:n.1332+83del
NM_172058.3:c.1698+83del	NP_742055.1:n.1698+83del
NM_172059.3:c.1593+83del	NP_742056.1:n.1593+83del
NM_172060.3:c.1599+83del	NP_742057.1:n.1599+83del
XM_011517481.1:c.1769+84del	XP_011515783.1:n.1769+84del
XM_011517482.1:c.1784+84del	XP_011515784.1:n.1784+84del
XM_011517483.1:c.1695+83del	XP_011515785.1:n.1695+83del
XM_011517484.1:c.1683+83del	XP_011515786.1:n.1683+83del
XM_011517485.1:c.1697+84del	XP_011515787.1:n.1697+84del
XM_011517486.1:c.1697+84del	XP_011515788.1:n.1697+84del
XM_011517487.1:c.1697+84del	XP_011515789.1:n.1697+84del
XM_011517488.1:c.1694+84del	XP_011515790.1:n.1694+84del
XM_011517489.1:c.1634+84del	XP_011515791.1:n.1634+84del
XM_011517490.1:c.1598+84del	XP_011515792.1:n.1598+84del
XM_011517491.1:c.1598+84del	XP_011515793.1:n.1598+84del
XM_011517492.1:c.1346+84del	XP_011515794.1:n.1346+84del
NM_172059.4:c.1680+83del	NP_742056.2:n.1680+83del
XM_011517483.2:c.1695+83del	XP_011515785.1:n.1695+83del
XM_011517484.3:c.1770+83del	XP_011515786.2:n.1770+83del
XM_017013201.1:c.1785+83del	XP_016868690.1:n.1785+83del
XM_017013202.1:c.1785+83del	XP_016868691.1:n.1785+83del
XM_017013203.2:c.1782+83del	XP_016868692.1:n.1782+83del
XM_017013204.2:c.1767+83del	XP_016868693.1:n.1767+83del
XM_017013205.2:c.1785+83del	XP_016868694.1:n.1785+83del
XM_017013206.1:c.1698+83del	XP_016868695.1:n.1698+83del
XM_017013207.2:c.1695+83del	XP_016868696.1:n.1695+83del
XM_017013208.2:c.1695+83del	XP_016868697.1:n.1695+83del
XM_017013210.2:c.1677+83del	XP_016868699.1:n.1677+83del
XM_017013211.2:c.1635+83del	XP_016868700.1:n.1635+83del
XM_017013212.2:c.1599+83del	XP_016868701.1:n.1599+83del
XM_017013213.1:c.1347+83del	XP_016868702.1:n.1347+83del
NM_000503.6:c.1698+83del MANE Select	NP_000494.2:n.1698+83del
NM_001288574.2:c.1680+83del	NP_001275503.1:n.1680+83del
NM_001288575.2:c.1332+83del	NP_001275504.1:n.1332+83del
NM_001370333.1:c.1785+83del	NP_001357262.1:n.1785+83del
NM_001370334.1:c.1698+83del	NP_001357263.1:n.1698+83del
NM_001370335.1:c.1698+83del	NP_001357264.1:n.1698+83del
NM_001370336.1:c.1677+83del	NP_001357265.1:n.1677+83del
NM_172058.4:c.1698+83del	NP_742055.1:n.1698+83del
NM_172059.5:c.1680+83del	NP_742056.2:n.1680+83del