Canonical Allele Identifier: CA1792716266
Gene: EYA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.71271860T= , CM000670.2:g.71271860T= GRCh38
NC_000008.10:g.72184095T= , CM000670.1:g.72184095T= GRCh37
NC_000008.9:g.72346649T= NCBI36
NG_011735.2:g.95373A=
NG_011735.3:g.281271A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340726.8:c.864A= MANE Select ENSP00000342626.3:p.Lys288=
ENST00000388741.7:c.762A= ENSP00000373393.2:p.Lys254=
ENST00000419131.6:c.849A= ENSP00000410176.1:p.Lys283=
ENST00000465115.6:c.*143A= ENSP00000428391.1:n.*143A=
ENST00000493349.2:c.100A=
ENST00000496494.6:n.1327A=
ENST00000642391.1:c.*631A= ENSP00000496700.1:n.*631A=
ENST00000643681.1:c.951A= ENSP00000495390.1:p.Lys317=
ENST00000644229.1:c.936A= ENSP00000494568.1:p.Lys312=
ENST00000644712.1:c.933A= ENSP00000496188.1:p.Lys311=
ENST00000645793.1:c.864A= ENSP00000496255.1:p.Lys288=
ENST00000647540.1:c.864A= ENSP00000494438.1:p.Lys288=
ENST00000303824.11:c.846A= ENSP00000303221.7:p.Lys282=
ENST00000340726.7:c.864A= ENSP00000342626.3:p.Lys288=
ENST00000388740.4:c.765A= ENSP00000373392.3:p.Lys255=
ENST00000388741.6:c.762A= ENSP00000373393.2:p.Lys254=
ENST00000388742.8:c.864A= ENSP00000373394.4:p.Lys288=
ENST00000388743.6:c.861A= ENSP00000373395.2:p.Lys287=
ENST00000419131.5:c.849A= ENSP00000410176.1:p.Lys283=
ENST00000465115.5:c.*143A= ENSP00000428391.1:n.*143A=
ENST00000493349.1:c.-220A= ENSP00000428517.1:n.-220A=
ENST00000496494.5:n.1359A=
NM_000503.5:c.864A= NP_000494.2:p.Lys288=
NM_001288574.1:c.846A= NP_001275503.1:p.Lys282=
NM_001288575.1:c.498A= NP_001275504.1:p.Lys166=
NM_172058.3:c.864A= NP_742055.1:p.Lys288=
NM_172059.3:c.849A= NP_742056.1:p.Lys283=
NM_172060.3:c.765A= NP_742057.1:p.Lys255=
XM_011517481.1:c.936A= XP_011515783.1:p.Lys312=
XM_011517482.1:c.951A= XP_011515784.1:p.Lys317=
XM_011517483.1:c.861A= XP_011515785.1:p.Lys287=
XM_011517484.1:c.849A= XP_011515786.1:p.Lys283=
XM_011517485.1:c.864A= XP_011515787.1:p.Lys288=
XM_011517486.1:c.864A= XP_011515788.1:p.Lys288=
XM_011517487.1:c.864A= XP_011515789.1:p.Lys288=
XM_011517488.1:c.861A= XP_011515790.1:p.Lys287=
XM_011517489.1:c.801A= XP_011515791.1:p.Lys267=
XM_011517490.1:c.765A= XP_011515792.1:p.Lys255=
XM_011517491.1:c.765A= XP_011515793.1:p.Lys255=
XM_011517492.1:c.513A= XP_011515794.1:p.Lys171=
NM_172059.4:c.936A= NP_742056.2:p.Lys312=
XM_011517483.2:c.861A= XP_011515785.1:p.Lys287=
XM_011517484.3:c.936A= XP_011515786.2:p.Lys312=
XM_017013201.1:c.951A= XP_016868690.1:p.Lys317=
XM_017013202.1:c.951A= XP_016868691.1:p.Lys317=
XM_017013203.2:c.948A= XP_016868692.1:p.Lys316=
XM_017013204.2:c.933A= XP_016868693.1:p.Lys311=
XM_017013205.2:c.951A= XP_016868694.1:p.Lys317=
XM_017013206.1:c.864A= XP_016868695.1:p.Lys288=
XM_017013207.2:c.951A= XP_016868696.1:p.Lys317=
XM_017013208.2:c.861A= XP_016868697.1:p.Lys287=
XM_017013210.2:c.933A= XP_016868699.1:p.Lys311=
XM_017013211.2:c.801A= XP_016868700.1:p.Lys267=
XM_017013212.2:c.765A= XP_016868701.1:p.Lys255=
XM_017013213.1:c.513A= XP_016868702.1:p.Lys171=
NM_000503.6:c.864A= MANE Select NP_000494.2:p.Lys288=
NM_001288574.2:c.846A= NP_001275503.1:p.Lys282=
NM_001288575.2:c.498A= NP_001275504.1:p.Lys166=
NM_001370333.1:c.951A= NP_001357262.1:p.Lys317=
NM_001370334.1:c.864A= NP_001357263.1:p.Lys288=
NM_001370335.1:c.864A= NP_001357264.1:p.Lys288=
NM_001370336.1:c.933A= NP_001357265.1:p.Lys311=
NM_172058.4:c.864A= NP_742055.1:p.Lys288=
NM_172059.5:c.936A= NP_742056.2:p.Lys312=