Canonical Allele Identifier: CA1905833011
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838416940
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130216_43130218dup , CM000672.2:g.43130216_43130218dup GRCh38
NC_000010.10:g.43625664_43625666dup , CM000672.1:g.43625664_43625666dup GRCh37
NC_000010.9:g.42945670_42945672dup NCBI36
NG_007489.1:g.58148_58150dup , LRG_518:g.58148_58150dup

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3462_*3464dup ENSP00000480088.2:n.*3462_*3464dup
ENST00000683007.1:n.6255_6257dup
ENST00000355710.8:c.*1947_*1949dup MANE Select ENSP00000347942.3:n.*1947_*1949dup
ENST00000355710.7:c.*1947_*1949dup ENSP00000347942.3:n.*1947_*1949dup
ENST00000615310.4:c.*2641_*2643dup ENSP00000480088.1:n.*2641_*2643dup
NM_020975.4:c.*1947_*1949dup , LRG_518t1:c.*1947_*1949dup NP_066124.1:n.*1947_*1949dup
XM_011540027.1:c.*715_*717dup XP_011538329.1:n.*715_*717dup
NM_020975.5:c.*1947_*1949dup NP_066124.1:n.*1947_*1949dup
NM_020975.6:c.*1947_*1949dup MANE Select NP_066124.1:n.*1947_*1949dup
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