Canonical Allele Identifier: CA665311359
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1339141960

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119915_43119946dup , CM000672.2:g.43119915_43119946dup GRCh38
NC_000010.10:g.43615363_43615394dup , CM000672.1:g.43615363_43615394dup GRCh37
NC_000010.9:g.42935369_42935400dup NCBI36
NG_007489.1:g.47847_47878dup , LRG_518:g.47847_47878dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2212-166_2212-135dup ENSP00000480088.2:n.2212-166_2212-135dup
ENST00000683007.1:n.2182-166_2182-135dup
ENST00000683872.1:n.2173-166_2173-135dup
ENST00000340058.6:c.2608-166_2608-135dup ENSP00000344798.4:n.2608-166_2608-135dup
ENST00000355710.8:c.2608-166_2608-135dup MANE Select ENSP00000347942.3:n.2608-166_2608-135dup
ENST00000671844.1:c.*1202-166_*1202-135dup ENSP00000500541.1:n.*1202-166_*1202-135dup
ENST00000672389.1:c.*1202-166_*1202-135dup ENSP00000500252.1:n.*1202-166_*1202-135dup
ENST00000340058.5:c.2608-166_2608-135dup ENSP00000344798.4:n.2608-166_2608-135dup
ENST00000355710.7:c.2608-166_2608-135dup ENSP00000347942.3:n.2608-166_2608-135dup
ENST00000615310.4:c.1334-166_1334-135dup ENSP00000480088.1:n.1334-166_1334-135dup
NM_020630.4:c.2608-166_2608-135dup , LRG_518t2:c.2608-166_2608-135dup NP_065681.1:n.2608-166_2608-135dup
NM_020975.4:c.2608-166_2608-135dup , LRG_518t1:c.2608-166_2608-135dup NP_066124.1:n.2608-166_2608-135dup
XM_011540027.1:c.2608-166_2608-135dup XP_011538329.1:n.2608-166_2608-135dup
NM_001355216.1:c.1846-166_1846-135dup NP_001342145.1:n.1846-166_1846-135dup
NM_020630.5:c.2608-166_2608-135dup NP_065681.1:n.2608-166_2608-135dup
NM_020975.5:c.2608-166_2608-135dup NP_066124.1:n.2608-166_2608-135dup
NM_020975.6:c.2608-166_2608-135dup MANE Select NP_066124.1:n.2608-166_2608-135dup
NM_020630.6:c.2608-166_2608-135dup NP_065681.1:n.2608-166_2608-135dup