Canonical Allele Identifier: CA2840894648
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113583dup , CM000672.2:g.43113583dup GRCh38
NC_000010.10:g.43609031dup , CM000672.1:g.43609031dup GRCh37
NC_000010.9:g.42929037dup NCBI36
NG_007489.1:g.41515dup , LRG_518:g.41515dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1391dup ENSP00000480088.2:p.Gly465TrpfsTer7
ENST00000683007.1:n.1361dup
ENST00000683872.1:n.548dup
ENST00000340058.6:c.1787dup ENSP00000344798.4:p.Gly597TrpfsTer7
ENST00000355710.8:c.1787dup MANE Select ENSP00000347942.3:p.Gly597TrpfsTer7
ENST00000671844.1:c.*381dup ENSP00000500541.1:n.*381dup
ENST00000672389.1:c.*381dup ENSP00000500252.1:n.*381dup
ENST00000340058.5:c.1787dup ENSP00000344798.4:p.Gly597TrpfsTer7
ENST00000355710.7:c.1787dup ENSP00000347942.3:p.Gly597TrpfsTer7
ENST00000498820.5:c.338dup ENSP00000419080.1:p.Gly114TrpfsTer7
ENST00000615310.4:c.1289+2351dup ENSP00000480088.1:n.1289+2351dup
NM_020630.4:c.1787dup , LRG_518t2:c.1787dup NP_065681.1:p.Gly597TrpfsTer7
NM_020975.4:c.1787dup , LRG_518t1:c.1787dup NP_066124.1:p.Gly597TrpfsTer7
XM_011540027.1:c.1787dup XP_011538329.1:p.Gly597TrpfsTer7
NM_001355216.1:c.1025dup NP_001342145.1:p.Gly343TrpfsTer7
NM_020630.5:c.1787dup NP_065681.1:p.Gly597TrpfsTer7
NM_020975.5:c.1787dup NP_066124.1:p.Gly597TrpfsTer7
NM_020975.6:c.1787dup MANE Select NP_066124.1:p.Gly597TrpfsTer7
NM_020630.6:c.1787dup NP_065681.1:p.Gly597TrpfsTer7