Canonical Allele Identifier: CA371465884

Gene: EYA1

Linked Data

• MyVariant Identifiers: chr8:g.72123426C>G (hg19) ; chr8:g.71211191C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.71211191C>G , CM000670.2:g.71211191C>G	GRCh38
NC_000008.10:g.72123426C>G , CM000670.1:g.72123426C>G	GRCh37
NC_000008.9:g.72285980C>G	NCBI36
NG_011735.2:g.156042G>C
NG_011735.3:g.341940G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340726.8:c.1663G>C MANE Select	ENSP00000342626.3:p.Gly555Arg
ENST00000388741.7:c.1561G>C	ENSP00000373393.2:p.Gly521Arg
ENST00000419131.6:c.1558G>C	ENSP00000410176.1:p.Gly520Arg
ENST00000465115.6:c.*942G>C	ENSP00000428391.1:n.*942G>C
ENST00000496494.6:n.2126G>C
ENST00000642391.1:c.*1340G>C	ENSP00000496700.1:n.*1340G>C
ENST00000643681.1:c.1750G>C	ENSP00000495390.1:p.Gly584Arg
ENST00000644229.1:c.1645G>C	ENSP00000494568.1:p.Gly549Arg
ENST00000644424.1:n.733G>C
ENST00000644712.1:c.1642G>C	ENSP00000496188.1:p.Gly548Arg
ENST00000645793.1:c.1663G>C	ENSP00000496255.1:p.Gly555Arg
ENST00000647540.1:c.1663G>C	ENSP00000494438.1:p.Gly555Arg
ENST00000303824.11:c.1645G>C	ENSP00000303221.7:p.Gly549Arg
ENST00000340726.7:c.1663G>C	ENSP00000342626.3:p.Gly555Arg
ENST00000388740.4:c.1564G>C	ENSP00000373392.3:p.Gly522Arg
ENST00000388741.6:c.1561G>C	ENSP00000373393.2:p.Gly521Arg
ENST00000388742.8:c.1663G>C	ENSP00000373394.4:p.Gly555Arg
ENST00000388743.6:c.1660G>C	ENSP00000373395.2:p.Gly554Arg
ENST00000419131.5:c.1558G>C	ENSP00000410176.1:p.Gly520Arg
ENST00000465115.5:c.*942G>C	ENSP00000428391.1:n.*942G>C
ENST00000496494.5:n.2158G>C
NM_000503.5:c.1663G>C	NP_000494.2:p.Gly555Arg
NM_001288574.1:c.1645G>C	NP_001275503.1:p.Gly549Arg
NM_001288575.1:c.1297G>C	NP_001275504.1:p.Gly433Arg
NM_172058.3:c.1663G>C	NP_742055.1:p.Gly555Arg
NM_172059.3:c.1558G>C	NP_742056.1:p.Gly520Arg
NM_172060.3:c.1564G>C	NP_742057.1:p.Gly522Arg
XM_011517481.1:c.1735G>C	XP_011515783.1:p.Gly579Arg
XM_011517482.1:c.1750G>C	XP_011515784.1:p.Gly584Arg
XM_011517483.1:c.1660G>C	XP_011515785.1:p.Gly554Arg
XM_011517484.1:c.1648G>C	XP_011515786.1:p.Gly550Arg
XM_011517485.1:c.1663G>C	XP_011515787.1:p.Gly555Arg
XM_011517486.1:c.1663G>C	XP_011515788.1:p.Gly555Arg
XM_011517487.1:c.1663G>C	XP_011515789.1:p.Gly555Arg
XM_011517488.1:c.1660G>C	XP_011515790.1:p.Gly554Arg
XM_011517489.1:c.1600G>C	XP_011515791.1:p.Gly534Arg
XM_011517490.1:c.1564G>C	XP_011515792.1:p.Gly522Arg
XM_011517491.1:c.1564G>C	XP_011515793.1:p.Gly522Arg
XM_011517492.1:c.1312G>C	XP_011515794.1:p.Gly438Arg
NM_172059.4:c.1645G>C	NP_742056.2:p.Gly549Arg
XM_011517483.2:c.1660G>C	XP_011515785.1:p.Gly554Arg
XM_011517484.3:c.1735G>C	XP_011515786.2:p.Gly579Arg
XM_017013201.1:c.1750G>C	XP_016868690.1:p.Gly584Arg
XM_017013202.1:c.1750G>C	XP_016868691.1:p.Gly584Arg
XM_017013203.2:c.1747G>C	XP_016868692.1:p.Gly583Arg
XM_017013204.2:c.1732G>C	XP_016868693.1:p.Gly578Arg
XM_017013205.2:c.1750G>C	XP_016868694.1:p.Gly584Arg
XM_017013206.1:c.1663G>C	XP_016868695.1:p.Gly555Arg
XM_017013207.2:c.1660G>C	XP_016868696.1:p.Gly554Arg
XM_017013208.2:c.1660G>C	XP_016868697.1:p.Gly554Arg
XM_017013210.2:c.1642G>C	XP_016868699.1:p.Gly548Arg
XM_017013211.2:c.1600G>C	XP_016868700.1:p.Gly534Arg
XM_017013212.2:c.1564G>C	XP_016868701.1:p.Gly522Arg
XM_017013213.1:c.1312G>C	XP_016868702.1:p.Gly438Arg
NM_000503.6:c.1663G>C MANE Select	NP_000494.2:p.Gly555Arg
NM_001288574.2:c.1645G>C	NP_001275503.1:p.Gly549Arg
NM_001288575.2:c.1297G>C	NP_001275504.1:p.Gly433Arg
NM_001370333.1:c.1750G>C	NP_001357262.1:p.Gly584Arg
NM_001370334.1:c.1663G>C	NP_001357263.1:p.Gly555Arg
NM_001370335.1:c.1663G>C	NP_001357264.1:p.Gly555Arg
NM_001370336.1:c.1642G>C	NP_001357265.1:p.Gly548Arg
NM_172058.4:c.1663G>C	NP_742055.1:p.Gly555Arg
NM_172059.5:c.1645G>C	NP_742056.2:p.Gly549Arg