Canonical Allele Identifier: CA2838160746

Gene: EYA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133452410C>A , CM000668.2:g.133452410C>A	GRCh38
NC_000006.11:g.133773548C>A , CM000668.1:g.133773548C>A	GRCh37
NC_000006.10:g.133815241C>A	NCBI36
NG_011596.1:g.216054C>A
NG_011596.2:g.216054C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525849.7:c.209-4146C>A	ENSP00000433219.1:n.209-4146C>A
ENST00000706301.1:c.208+5656C>A	ENSP00000516341.1:n.208+5656C>A
ENST00000355167.8:c.208+5656C>A	ENSP00000347294.4:n.208+5656C>A
ENST00000683664.1:n.244-4146C>A
ENST00000684773.1:c.-200-4146C>A	ENSP00000506812.1:n.-200-4146C>A
ENST00000355286.12:c.278-4146C>A MANE Select	ENSP00000347434.7:n.278-4146C>A
ENST00000431403.3:c.209-4146C>A	ENSP00000404558.3:n.209-4146C>A
ENST00000525614.2:n.545+5656C>A
ENST00000525849.6:c.209-4146C>A	ENSP00000433219.1:n.209-4146C>A
ENST00000355167.7:c.278-4146C>A	ENSP00000347294.3:n.278-4146C>A
ENST00000355286.10:c.209-4146C>A	ENSP00000347434.6:n.209-4146C>A
ENST00000367895.9:c.278-4146C>A	ENSP00000356870.5:n.278-4146C>A
ENST00000421413.6:n.380-4146C>A
ENST00000430974.6:c.208+5656C>A	ENSP00000388670.2:n.208+5656C>A
ENST00000431403.2:c.278-4146C>A	ENSP00000404558.2:n.278-4146C>A
ENST00000452339.6:c.208+5656C>A	ENSP00000395916.2:n.208+5656C>A
ENST00000525614.1:n.545+5656C>A
ENST00000525849.5:c.209-4146C>A	ENSP00000433219.1:n.209-4146C>A
ENST00000531861.5:n.278-4146C>A
ENST00000531901.5:c.278-4146C>A	ENSP00000432770.1:n.278-4146C>A
NM_001301012.1:c.208+5656C>A	NP_001287941.1:n.208+5656C>A
NM_001301013.1:c.278-4146C>A	NP_001287942.1:n.278-4146C>A
NM_004100.4:c.278-4146C>A	NP_004091.3:n.278-4146C>A
NM_172103.3:c.209-4146C>A	NP_742101.2:n.209-4146C>A
NM_172105.3:c.278-4146C>A	NP_742103.1:n.278-4146C>A
XM_005266851.3:c.278-4146C>A	XP_005266908.1:n.278-4146C>A
XM_005266852.3:c.278-4146C>A	XP_005266909.1:n.278-4146C>A
XM_005266853.3:c.209-4146C>A	XP_005266910.1:n.209-4146C>A
XM_011535540.1:c.209-4146C>A	XP_011533842.1:n.209-4146C>A
XM_011535541.1:c.209-4161C>A	XP_011533843.1:n.209-4161C>A
XM_011535542.1:c.208+5656C>A	XP_011533844.1:n.208+5656C>A
XM_005266851.5:c.278-4146C>A	XP_005266908.1:n.278-4146C>A
XM_005266853.5:c.209-4146C>A	XP_005266910.1:n.209-4146C>A
XM_017010368.2:c.278-4146C>A	XP_016865857.1:n.278-4146C>A
XM_017010369.2:c.278-4146C>A	XP_016865858.1:n.278-4146C>A
XM_017010370.2:c.209-4146C>A	XP_016865859.1:n.209-4146C>A
XM_017010371.2:c.209-4161C>A	XP_016865860.1:n.209-4161C>A
XM_017010372.2:c.208+5656C>A	XP_016865861.1:n.208+5656C>A
XM_017010373.2:c.208+5656C>A	XP_016865862.1:n.208+5656C>A
XM_017010374.2:c.208+5656C>A	XP_016865863.1:n.208+5656C>A
XM_017010375.1:c.208+5656C>A	XP_016865864.1:n.208+5656C>A
XR_001743219.2:n.440-4146C>A
XR_001743220.2:n.440-4146C>A
NM_004100.5:c.278-4146C>A MANE Select	NP_004091.3:n.278-4146C>A
NM_001370458.1:c.209-4146C>A	NP_001357387.1:n.209-4146C>A
NM_001370459.1:c.208+5656C>A	NP_001357388.1:n.208+5656C>A
NM_001301012.2:c.208+5656C>A	NP_001287941.1:n.208+5656C>A
NM_001301013.2:c.278-4146C>A	NP_001287942.1:n.278-4146C>A
NM_172103.4:c.209-4146C>A	NP_742101.2:n.209-4146C>A
NM_172105.4:c.278-4146C>A	NP_742103.1:n.278-4146C>A