Canonical Allele Identifier: CA2695211983
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43118467del , CM000672.2:g.43118467del GRCh38
NC_000010.10:g.43613915del , CM000672.1:g.43613915del GRCh37
NC_000010.9:g.42933921del NCBI36
NG_007489.1:g.46399del , LRG_518:g.46399del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1983del ENSP00000480088.2:p.Cys662AlafsTer?
ENST00000683007.1:n.1953del
ENST00000683872.1:n.1944del
ENST00000340058.6:c.2379del ENSP00000344798.4:p.Cys794AlafsTer?
ENST00000355710.8:c.2379del MANE Select ENSP00000347942.3:p.Cys794AlafsTer?
ENST00000671844.1:c.*973del ENSP00000500541.1:n.*973del
ENST00000672389.1:c.*973del ENSP00000500252.1:n.*973del
ENST00000340058.5:c.2379del ENSP00000344798.4:p.Cys794AlafsTer?
ENST00000355710.7:c.2379del ENSP00000347942.3:p.Cys794AlafsTer?
ENST00000615310.4:c.1290-1235del ENSP00000480088.1:n.1290-1235del
NM_020630.4:c.2379del , LRG_518t2:c.2379del NP_065681.1:p.Cys794AlafsTer?
NM_020975.4:c.2379del , LRG_518t1:c.2379del NP_066124.1:p.Cys794AlafsTer?
XM_011540027.1:c.2379del XP_011538329.1:p.Cys794AlafsTer?
NM_001355216.1:c.1617del NP_001342145.1:p.Cys540AlafsTer?
NM_020630.5:c.2379del NP_065681.1:p.Cys794AlafsTer?
NM_020975.5:c.2379del NP_066124.1:p.Cys794AlafsTer?
NM_020975.6:c.2379del MANE Select NP_066124.1:p.Cys794AlafsTer?
NM_020630.6:c.2379del NP_065681.1:p.Cys794AlafsTer?