Canonical Allele Identifier: CA1647271908
Gene: EPHA7 HGNC NCBI

Linked Data

dbSNP Id: rs1772806592

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.93298725_93298726del , CM000668.2:g.93298725_93298726del GRCh38
NC_000006.11:g.94008443_94008444del , CM000668.1:g.94008443_94008444del GRCh37
NC_000006.10:g.94065164_94065165del NCBI36
NG_033944.1:g.125857_125858del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369303.9:c.1325-26304_1325-26303del MANE Select ENSP00000358309.4:n.1325-26304_1325-26303del
ENST00000679565.1:c.1325-26304_1325-26303del ENSP00000506548.1:n.1325-26304_1325-26303del
ENST00000679915.1:n.1537-26304_1537-26303del
ENST00000680082.1:c.1325-26304_1325-26303del ENSP00000506654.1:n.1325-26304_1325-26303del
ENST00000680190.1:c.1097-26304_1097-26303del ENSP00000505937.1:n.1097-26304_1097-26303del
ENST00000680224.1:c.1325-26304_1325-26303del ENSP00000506130.1:n.1325-26304_1325-26303del
ENST00000680473.1:n.1563-26304_1563-26303del
ENST00000680813.1:n.567-26304_567-26303del
ENST00000680953.1:c.1097-26304_1097-26303del ENSP00000505682.1:n.1097-26304_1097-26303del
ENST00000681130.1:c.1325-26304_1325-26303del ENSP00000505801.1:n.1325-26304_1325-26303del
ENST00000681532.1:c.1325-26304_1325-26303del ENSP00000505741.1:n.1325-26304_1325-26303del
ENST00000681647.1:n.1536-14342_1536-14341del
ENST00000369303.8:c.1325-26304_1325-26303del ENSP00000358309.4:n.1325-26304_1325-26303del
NM_001288629.1:c.1325-26304_1325-26303del NP_001275558.1:n.1325-26304_1325-26303del
NM_004440.3:c.1325-26304_1325-26303del NP_004431.1:n.1325-26304_1325-26303del
XM_005248669.1:c.1325-26304_1325-26303del XP_005248726.1:n.1325-26304_1325-26303del
XM_005248671.1:c.1325-26304_1325-26303del XP_005248728.1:n.1325-26304_1325-26303del
XM_005248669.3:c.1325-26304_1325-26303del XP_005248726.1:n.1325-26304_1325-26303del
XM_005248671.3:c.1325-26304_1325-26303del XP_005248728.1:n.1325-26304_1325-26303del
XM_017010365.2:c.1325-26304_1325-26303del XP_016865854.1:n.1325-26304_1325-26303del
XR_001743218.2:n.1568-26304_1568-26303del
NM_004440.4:c.1325-26304_1325-26303del MANE Select NP_004431.1:n.1325-26304_1325-26303del
NM_001288629.2:c.1325-26304_1325-26303del NP_001275558.1:n.1325-26304_1325-26303del
NM_001376465.1:c.1325-26304_1325-26303del NP_001363394.1:n.1325-26304_1325-26303del
NM_001376466.1:c.1325-26304_1325-26303del NP_001363395.1:n.1325-26304_1325-26303del
NM_001376467.1:c.1325-26304_1325-26303del NP_001363396.1:n.1325-26304_1325-26303del
NM_001376468.1:c.1325-26304_1325-26303del NP_001363397.1:n.1325-26304_1325-26303del
NM_001376470.1:c.1097-26304_1097-26303del NP_001363399.1:n.1097-26304_1097-26303del
NM_001376471.1:c.1097-26304_1097-26303del NP_001363400.1:n.1097-26304_1097-26303del
NR_164810.1:n.1543-26304_1543-26303del