Canonical Allele Identifier: CA371466356

Gene: EYA1

Linked Data

• MyVariant Identifiers: chr8:g.72127868G>T (hg19) ; chr8:g.71215633G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.71215633G>T , CM000670.2:g.71215633G>T	GRCh38
NC_000008.10:g.72127868G>T , CM000670.1:g.72127868G>T	GRCh37
NC_000008.9:g.72290422G>T	NCBI36
NG_011735.2:g.151600C>A
NG_011735.3:g.337498C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340726.8:c.1456C>A MANE Select	ENSP00000342626.3:p.Leu486Ile
ENST00000388741.7:c.1354C>A	ENSP00000373393.2:p.Leu452Ile
ENST00000419131.6:c.1351C>A	ENSP00000410176.1:p.Leu451Ile
ENST00000465115.6:c.*735C>A	ENSP00000428391.1:n.*735C>A
ENST00000493349.2:c.846C>A
ENST00000496494.6:n.1919C>A
ENST00000642391.1:c.*1133C>A	ENSP00000496700.1:n.*1133C>A
ENST00000643681.1:c.1543C>A	ENSP00000495390.1:p.Leu515Ile
ENST00000644229.1:c.1438C>A	ENSP00000494568.1:p.Leu480Ile
ENST00000644424.1:n.526C>A
ENST00000644712.1:c.1435C>A	ENSP00000496188.1:p.Leu479Ile
ENST00000645793.1:c.1456C>A	ENSP00000496255.1:p.Leu486Ile
ENST00000647540.1:c.1456C>A	ENSP00000494438.1:p.Leu486Ile
ENST00000303824.11:c.1438C>A	ENSP00000303221.7:p.Leu480Ile
ENST00000340726.7:c.1456C>A	ENSP00000342626.3:p.Leu486Ile
ENST00000388740.4:c.1357C>A	ENSP00000373392.3:p.Leu453Ile
ENST00000388741.6:c.1354C>A	ENSP00000373393.2:p.Leu452Ile
ENST00000388742.8:c.1456C>A	ENSP00000373394.4:p.Leu486Ile
ENST00000388743.6:c.1453C>A	ENSP00000373395.2:p.Leu485Ile
ENST00000419131.5:c.1351C>A	ENSP00000410176.1:p.Leu451Ile
ENST00000465115.5:c.*735C>A	ENSP00000428391.1:n.*735C>A
ENST00000493349.1:c.*401C>A	ENSP00000428517.1:n.*401C>A
ENST00000496494.5:n.1951C>A
NM_000503.5:c.1456C>A	NP_000494.2:p.Leu486Ile
NM_001288574.1:c.1438C>A	NP_001275503.1:p.Leu480Ile
NM_001288575.1:c.1090C>A	NP_001275504.1:p.Leu364Ile
NM_172058.3:c.1456C>A	NP_742055.1:p.Leu486Ile
NM_172059.3:c.1351C>A	NP_742056.1:p.Leu451Ile
NM_172060.3:c.1357C>A	NP_742057.1:p.Leu453Ile
XM_011517481.1:c.1528C>A	XP_011515783.1:p.Leu510Ile
XM_011517482.1:c.1543C>A	XP_011515784.1:p.Leu515Ile
XM_011517483.1:c.1453C>A	XP_011515785.1:p.Leu485Ile
XM_011517484.1:c.1441C>A	XP_011515786.1:p.Leu481Ile
XM_011517485.1:c.1456C>A	XP_011515787.1:p.Leu486Ile
XM_011517486.1:c.1456C>A	XP_011515788.1:p.Leu486Ile
XM_011517487.1:c.1456C>A	XP_011515789.1:p.Leu486Ile
XM_011517488.1:c.1453C>A	XP_011515790.1:p.Leu485Ile
XM_011517489.1:c.1393C>A	XP_011515791.1:p.Leu465Ile
XM_011517490.1:c.1357C>A	XP_011515792.1:p.Leu453Ile
XM_011517491.1:c.1357C>A	XP_011515793.1:p.Leu453Ile
XM_011517492.1:c.1105C>A	XP_011515794.1:p.Leu369Ile
NM_172059.4:c.1438C>A	NP_742056.2:p.Leu480Ile
XM_011517483.2:c.1453C>A	XP_011515785.1:p.Leu485Ile
XM_011517484.3:c.1528C>A	XP_011515786.2:p.Leu510Ile
XM_017013201.1:c.1543C>A	XP_016868690.1:p.Leu515Ile
XM_017013202.1:c.1543C>A	XP_016868691.1:p.Leu515Ile
XM_017013203.2:c.1540C>A	XP_016868692.1:p.Leu514Ile
XM_017013204.2:c.1525C>A	XP_016868693.1:p.Leu509Ile
XM_017013205.2:c.1543C>A	XP_016868694.1:p.Leu515Ile
XM_017013206.1:c.1456C>A	XP_016868695.1:p.Leu486Ile
XM_017013207.2:c.1453C>A	XP_016868696.1:p.Leu485Ile
XM_017013208.2:c.1453C>A	XP_016868697.1:p.Leu485Ile
XM_017013210.2:c.1435C>A	XP_016868699.1:p.Leu479Ile
XM_017013211.2:c.1393C>A	XP_016868700.1:p.Leu465Ile
XM_017013212.2:c.1357C>A	XP_016868701.1:p.Leu453Ile
XM_017013213.1:c.1105C>A	XP_016868702.1:p.Leu369Ile
NM_000503.6:c.1456C>A MANE Select	NP_000494.2:p.Leu486Ile
NM_001288574.2:c.1438C>A	NP_001275503.1:p.Leu480Ile
NM_001288575.2:c.1090C>A	NP_001275504.1:p.Leu364Ile
NM_001370333.1:c.1543C>A	NP_001357262.1:p.Leu515Ile
NM_001370334.1:c.1456C>A	NP_001357263.1:p.Leu486Ile
NM_001370335.1:c.1456C>A	NP_001357264.1:p.Leu486Ile
NM_001370336.1:c.1435C>A	NP_001357265.1:p.Leu479Ile
NM_172058.4:c.1456C>A	NP_742055.1:p.Leu486Ile
NM_172059.5:c.1438C>A	NP_742056.2:p.Leu480Ile