Canonical Allele Identifier: CA927682424
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838416541

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130206_43130222dup , CM000672.2:g.43130206_43130222dup GRCh38
NC_000010.10:g.43625654_43625670dup , CM000672.1:g.43625654_43625670dup GRCh37
NC_000010.9:g.42945660_42945676dup NCBI36
NG_007489.1:g.58138_58154dup , LRG_518:g.58138_58154dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.*3452_*3468dup ENSP00000480088.2:n.*3452_*3468dup
ENST00000683007.1:n.6245_6261dup
ENST00000355710.8:c.*1937_*1953dup MANE Select ENSP00000347942.3:n.*1937_*1953dup
ENST00000355710.7:c.*1937_*1953dup ENSP00000347942.3:n.*1937_*1953dup
ENST00000615310.4:c.*2631_*2647dup ENSP00000480088.1:n.*2631_*2647dup
NM_020975.4:c.*1937_*1953dup , LRG_518t1:c.*1937_*1953dup NP_066124.1:n.*1937_*1953dup
XM_011540027.1:c.*705_*721dup XP_011538329.1:n.*705_*721dup
NM_020975.5:c.*1937_*1953dup NP_066124.1:n.*1937_*1953dup
NM_020975.6:c.*1937_*1953dup MANE Select NP_066124.1:n.*1937_*1953dup