Canonical Allele Identifier: CA2608875631
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119826_43119840dup , CM000672.2:g.43119826_43119840dup GRCh38
NC_000010.10:g.43615274_43615288dup , CM000672.1:g.43615274_43615288dup GRCh37
NC_000010.9:g.42935280_42935294dup NCBI36
NG_007489.1:g.47758_47772dup , LRG_518:g.47758_47772dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2211+81_2211+95dup ENSP00000480088.2:n.2211+81_2211+95dup
ENST00000683007.1:n.2181+81_2181+95dup
ENST00000683872.1:n.2172+81_2172+95dup
ENST00000340058.6:c.2607+81_2607+95dup ENSP00000344798.4:n.2607+81_2607+95dup
ENST00000355710.8:c.2607+81_2607+95dup MANE Select ENSP00000347942.3:n.2607+81_2607+95dup
ENST00000671844.1:c.*1201+81_*1201+95dup ENSP00000500541.1:n.*1201+81_*1201+95dup
ENST00000672389.1:c.*1201+81_*1201+95dup ENSP00000500252.1:n.*1201+81_*1201+95dup
ENST00000340058.5:c.2607+81_2607+95dup ENSP00000344798.4:n.2607+81_2607+95dup
ENST00000355710.7:c.2607+81_2607+95dup ENSP00000347942.3:n.2607+81_2607+95dup
ENST00000615310.4:c.1333+81_1333+95dup ENSP00000480088.1:n.1333+81_1333+95dup
NM_020630.4:c.2607+81_2607+95dup , LRG_518t2:c.2607+81_2607+95dup NP_065681.1:n.2607+81_2607+95dup
NM_020975.4:c.2607+81_2607+95dup , LRG_518t1:c.2607+81_2607+95dup NP_066124.1:n.2607+81_2607+95dup
XM_011540027.1:c.2607+81_2607+95dup XP_011538329.1:n.2607+81_2607+95dup
NM_001355216.1:c.1845+81_1845+95dup NP_001342145.1:n.1845+81_1845+95dup
NM_020630.5:c.2607+81_2607+95dup NP_065681.1:n.2607+81_2607+95dup
NM_020975.5:c.2607+81_2607+95dup NP_066124.1:n.2607+81_2607+95dup
NM_020975.6:c.2607+81_2607+95dup MANE Select NP_066124.1:n.2607+81_2607+95dup
NM_020630.6:c.2607+81_2607+95dup NP_065681.1:n.2607+81_2607+95dup