Canonical Allele Identifier: CA461327872

Gene: EYA1

Linked Data

• MyVariant Identifiers: chr8:g.72211373G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.71299138G>A , CM000670.2:g.71299138G>A	GRCh38
NC_000008.10:g.72211373G>A , CM000670.1:g.72211373G>A	GRCh37
NC_000008.9:g.72373927G>A	NCBI36
NG_011735.2:g.68095C>T
NG_011735.3:g.253993C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340726.8:c.735C>T MANE Select	ENSP00000342626.3:p.Thr245=
ENST00000388741.7:c.633C>T	ENSP00000373393.2:p.Thr211=
ENST00000419131.6:c.720C>T	ENSP00000410176.1:p.Thr240=
ENST00000465115.6:c.*14C>T	ENSP00000428391.1:n.*14C>T
ENST00000496494.6:n.1198C>T
ENST00000642391.1:c.*502C>T	ENSP00000496700.1:n.*502C>T
ENST00000643681.1:c.822C>T	ENSP00000495390.1:p.Thr274=
ENST00000644229.1:c.807C>T	ENSP00000494568.1:p.Thr269=
ENST00000644712.1:c.804C>T	ENSP00000496188.1:p.Thr268=
ENST00000645793.1:c.735C>T	ENSP00000496255.1:p.Thr245=
ENST00000647540.1:c.735C>T	ENSP00000494438.1:p.Thr245=
ENST00000303824.11:c.717C>T	ENSP00000303221.7:p.Thr239=
ENST00000340726.7:c.735C>T	ENSP00000342626.3:p.Thr245=
ENST00000388740.4:c.636C>T	ENSP00000373392.3:p.Thr212=
ENST00000388741.6:c.633C>T	ENSP00000373393.2:p.Thr211=
ENST00000388742.8:c.735C>T	ENSP00000373394.4:p.Thr245=
ENST00000388743.6:c.732C>T	ENSP00000373395.2:p.Thr244=
ENST00000419131.5:c.720C>T	ENSP00000410176.1:p.Thr240=
ENST00000465115.5:c.*14C>T	ENSP00000428391.1:n.*14C>T
ENST00000496494.5:n.1230C>T
NM_000503.5:c.735C>T	NP_000494.2:p.Thr245=
NM_001288574.1:c.717C>T	NP_001275503.1:p.Thr239=
NM_001288575.1:c.369C>T	NP_001275504.1:p.Thr123=
NM_172058.3:c.735C>T	NP_742055.1:p.Thr245=
NM_172059.3:c.720C>T	NP_742056.1:p.Thr240=
NM_172060.3:c.636C>T	NP_742057.1:p.Thr212=
XM_011517481.1:c.807C>T	XP_011515783.1:p.Thr269=
XM_011517482.1:c.822C>T	XP_011515784.1:p.Thr274=
XM_011517483.1:c.732C>T	XP_011515785.1:p.Thr244=
XM_011517484.1:c.720C>T	XP_011515786.1:p.Thr240=
XM_011517485.1:c.735C>T	XP_011515787.1:p.Thr245=
XM_011517486.1:c.735C>T	XP_011515788.1:p.Thr245=
XM_011517487.1:c.735C>T	XP_011515789.1:p.Thr245=
XM_011517488.1:c.732C>T	XP_011515790.1:p.Thr244=
XM_011517489.1:c.672C>T	XP_011515791.1:p.Thr224=
XM_011517490.1:c.636C>T	XP_011515792.1:p.Thr212=
XM_011517491.1:c.636C>T	XP_011515793.1:p.Thr212=
XM_011517492.1:c.384C>T	XP_011515794.1:p.Thr128=
NM_172059.4:c.807C>T	NP_742056.2:p.Thr269=
XM_011517483.2:c.732C>T	XP_011515785.1:p.Thr244=
XM_011517484.3:c.807C>T	XP_011515786.2:p.Thr269=
XM_017013201.1:c.822C>T	XP_016868690.1:p.Thr274=
XM_017013202.1:c.822C>T	XP_016868691.1:p.Thr274=
XM_017013203.2:c.819C>T	XP_016868692.1:p.Thr273=
XM_017013204.2:c.804C>T	XP_016868693.1:p.Thr268=
XM_017013205.2:c.822C>T	XP_016868694.1:p.Thr274=
XM_017013206.1:c.735C>T	XP_016868695.1:p.Thr245=
XM_017013207.2:c.822C>T	XP_016868696.1:p.Thr274=
XM_017013208.2:c.732C>T	XP_016868697.1:p.Thr244=
XM_017013210.2:c.804C>T	XP_016868699.1:p.Thr268=
XM_017013211.2:c.672C>T	XP_016868700.1:p.Thr224=
XM_017013212.2:c.636C>T	XP_016868701.1:p.Thr212=
XM_017013213.1:c.384C>T	XP_016868702.1:p.Thr128=
NM_000503.6:c.735C>T MANE Select	NP_000494.2:p.Thr245=
NM_001288574.2:c.717C>T	NP_001275503.1:p.Thr239=
NM_001288575.2:c.369C>T	NP_001275504.1:p.Thr123=
NM_001370333.1:c.822C>T	NP_001357262.1:p.Thr274=
NM_001370334.1:c.735C>T	NP_001357263.1:p.Thr245=
NM_001370335.1:c.735C>T	NP_001357264.1:p.Thr245=
NM_001370336.1:c.804C>T	NP_001357265.1:p.Thr268=
NM_172058.4:c.735C>T	NP_742055.1:p.Thr245=
NM_172059.5:c.807C>T	NP_742056.2:p.Thr269=