Canonical Allele Identifier: CA1664921853

Gene: EYA4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.133247575T>G , CM000668.2:g.133247575T>G	GRCh38
NC_000006.11:g.133568713T>G , CM000668.1:g.133568713T>G	GRCh37
NC_000006.10:g.133610406T>G	NCBI36
NG_011596.1:g.11219T>G
NG_011596.2:g.11219T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525849.7:c.-66+5826T>G	ENSP00000433219.1:n.-66+5826T>G
ENST00000706301.1:c.-66+5826T>G	ENSP00000516341.1:n.-66+5826T>G
ENST00000355167.8:c.-66+5826T>G	ENSP00000347294.4:n.-66+5826T>G
ENST00000682730.1:n.925T>G
ENST00000683361.1:n.1255T>G
ENST00000683421.1:n.911T>G
ENST00000683422.1:n.1020T>G
ENST00000683580.1:n.1195T>G
ENST00000684040.1:n.1159T>G
ENST00000684097.1:n.1077T>G
ENST00000684425.1:n.1074T>G
ENST00000684513.1:n.928T>G
ENST00000684773.1:c.-424+5826T>G	ENSP00000506812.1:n.-424+5826T>G
ENST00000355286.12:c.-66+5826T>G MANE Select	ENSP00000347434.7:n.-66+5826T>G
ENST00000431403.3:c.-66+5826T>G	ENSP00000404558.3:n.-66+5826T>G
ENST00000525849.6:c.-66+5826T>G	ENSP00000433219.1:n.-66+5826T>G
ENST00000355167.7:c.-66+5826T>G	ENSP00000347294.3:n.-66+5826T>G
ENST00000355286.10:c.-66+5826T>G	ENSP00000347434.6:n.-66+5826T>G
ENST00000367895.9:c.-66+5826T>G	ENSP00000356870.5:n.-66+5826T>G
ENST00000430974.6:c.-66+5826T>G	ENSP00000388670.2:n.-66+5826T>G
ENST00000441015.1:n.1221T>G
ENST00000452339.6:c.-66+5826T>G	ENSP00000395916.2:n.-66+5826T>G
ENST00000525849.5:c.-66+5826T>G	ENSP00000433219.1:n.-66+5826T>G
ENST00000531901.5:c.-66+5826T>G	ENSP00000432770.1:n.-66+5826T>G
NM_001301012.1:c.-66+5826T>G	NP_001287941.1:n.-66+5826T>G
NM_001301013.1:c.-66+5826T>G	NP_001287942.1:n.-66+5826T>G
NM_004100.4:c.-66+5826T>G	NP_004091.3:n.-66+5826T>G
NM_172103.3:c.-66+5826T>G	NP_742101.2:n.-66+5826T>G
NM_172105.3:c.-66+5826T>G	NP_742103.1:n.-66+5826T>G
XM_005266851.3:c.-66+5826T>G	XP_005266908.1:n.-66+5826T>G
XM_005266852.3:c.-66+5826T>G	XP_005266909.1:n.-66+5826T>G
XM_005266853.3:c.-66+5826T>G	XP_005266910.1:n.-66+5826T>G
XM_011535540.1:c.-66+5826T>G	XP_011533842.1:n.-66+5826T>G
XM_011535541.1:c.-66+5826T>G	XP_011533843.1:n.-66+5826T>G
XM_011535542.1:c.-66+5826T>G	XP_011533844.1:n.-66+5826T>G
XM_005266851.5:c.-66+5826T>G	XP_005266908.1:n.-66+5826T>G
XM_005266853.5:c.-66+5826T>G	XP_005266910.1:n.-66+5826T>G
XM_017010368.2:c.-66+5826T>G	XP_016865857.1:n.-66+5826T>G
XM_017010369.2:c.-66+5826T>G	XP_016865858.1:n.-66+5826T>G
XM_017010370.2:c.-66+5826T>G	XP_016865859.1:n.-66+5826T>G
XM_017010371.2:c.-66+5826T>G	XP_016865860.1:n.-66+5826T>G
XM_017010372.2:c.-66+5826T>G	XP_016865861.1:n.-66+5826T>G
XM_017010373.2:c.-66+5826T>G	XP_016865862.1:n.-66+5826T>G
XM_017010374.2:c.-66+5826T>G	XP_016865863.1:n.-66+5826T>G
XM_017010375.1:c.-66+5826T>G	XP_016865864.1:n.-66+5826T>G
XR_001743219.2:n.97+5826T>G
XR_001743220.2:n.97+5826T>G
NM_004100.5:c.-66+5826T>G MANE Select	NP_004091.3:n.-66+5826T>G
NM_001370458.1:c.-66+5826T>G	NP_001357387.1:n.-66+5826T>G
NM_001370459.1:c.-66+5826T>G	NP_001357388.1:n.-66+5826T>G
NM_001301012.2:c.-66+5826T>G	NP_001287941.1:n.-66+5826T>G
NM_001301013.2:c.-66+5826T>G	NP_001287942.1:n.-66+5826T>G
NM_172103.4:c.-66+5826T>G	NP_742101.2:n.-66+5826T>G
NM_172105.4:c.-66+5826T>G	NP_742103.1:n.-66+5826T>G