Canonical Allele Identifier: CA2608875477
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119448_43119452del , CM000672.2:g.43119448_43119452del GRCh38
NC_000010.10:g.43614896_43614900del , CM000672.1:g.43614896_43614900del GRCh37
NC_000010.9:g.42934902_42934906del NCBI36
NG_007489.1:g.47380_47384del , LRG_518:g.47380_47384del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1997-83_1997-79del ENSP00000480088.2:n.1997-83_1997-79del
ENST00000683007.1:n.1967-83_1967-79del
ENST00000683872.1:n.1958-83_1958-79del
ENST00000340058.6:c.2393-83_2393-79del ENSP00000344798.4:n.2393-83_2393-79del
ENST00000355710.8:c.2393-83_2393-79del MANE Select ENSP00000347942.3:n.2393-83_2393-79del
ENST00000671844.1:c.*987-83_*987-79del ENSP00000500541.1:n.*987-83_*987-79del
ENST00000672389.1:c.*987-83_*987-79del ENSP00000500252.1:n.*987-83_*987-79del
ENST00000340058.5:c.2393-83_2393-79del ENSP00000344798.4:n.2393-83_2393-79del
ENST00000355710.7:c.2393-83_2393-79del ENSP00000347942.3:n.2393-83_2393-79del
ENST00000615310.4:c.1290-254_1290-250del ENSP00000480088.1:n.1290-254_1290-250del
NM_020630.4:c.2393-83_2393-79del , LRG_518t2:c.2393-83_2393-79del NP_065681.1:n.2393-83_2393-79del
NM_020975.4:c.2393-83_2393-79del , LRG_518t1:c.2393-83_2393-79del NP_066124.1:n.2393-83_2393-79del
XM_011540027.1:c.2393-83_2393-79del XP_011538329.1:n.2393-83_2393-79del
NM_001355216.1:c.1631-83_1631-79del NP_001342145.1:n.1631-83_1631-79del
NM_020630.5:c.2393-83_2393-79del NP_065681.1:n.2393-83_2393-79del
NM_020975.5:c.2393-83_2393-79del NP_066124.1:n.2393-83_2393-79del
NM_020975.6:c.2393-83_2393-79del MANE Select NP_066124.1:n.2393-83_2393-79del
NM_020630.6:c.2393-83_2393-79del NP_065681.1:n.2393-83_2393-79del