Canonical Allele Identifier: CA5476483
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs777315635

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119797_43119826del , CM000672.2:g.43119797_43119826del GRCh38
NC_000010.10:g.43615245_43615274del , CM000672.1:g.43615245_43615274del GRCh37
NC_000010.9:g.42935251_42935280del NCBI36
NG_007489.1:g.47729_47758del , LRG_518:g.47729_47758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2211+52_2211+81del ENSP00000480088.2:n.2211+52_2211+81del
ENST00000683007.1:n.2181+52_2181+81del
ENST00000683872.1:n.2172+52_2172+81del
ENST00000340058.6:c.2607+52_2607+81del ENSP00000344798.4:n.2607+52_2607+81del
ENST00000355710.8:c.2607+52_2607+81del MANE Select ENSP00000347942.3:n.2607+52_2607+81del
ENST00000671844.1:c.*1201+52_*1201+81del ENSP00000500541.1:n.*1201+52_*1201+81del
ENST00000672389.1:c.*1201+52_*1201+81del ENSP00000500252.1:n.*1201+52_*1201+81del
ENST00000340058.5:c.2607+52_2607+81del ENSP00000344798.4:n.2607+52_2607+81del
ENST00000355710.7:c.2607+52_2607+81del ENSP00000347942.3:n.2607+52_2607+81del
ENST00000615310.4:c.1333+52_1333+81del ENSP00000480088.1:n.1333+52_1333+81del
NM_020630.4:c.2607+52_2607+81del , LRG_518t2:c.2607+52_2607+81del NP_065681.1:n.2607+52_2607+81del
NM_020975.4:c.2607+52_2607+81del , LRG_518t1:c.2607+52_2607+81del NP_066124.1:n.2607+52_2607+81del
XM_011540027.1:c.2607+52_2607+81del XP_011538329.1:n.2607+52_2607+81del
NM_001355216.1:c.1845+52_1845+81del NP_001342145.1:n.1845+52_1845+81del
NM_020630.5:c.2607+52_2607+81del NP_065681.1:n.2607+52_2607+81del
NM_020975.5:c.2607+52_2607+81del NP_066124.1:n.2607+52_2607+81del
NM_020975.6:c.2607+52_2607+81del MANE Select NP_066124.1:n.2607+52_2607+81del
NM_020630.6:c.2607+52_2607+81del NP_065681.1:n.2607+52_2607+81del