Canonical Allele Identifier: CA16602760
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 376314
ClinVar RCV Id: RCV000433213 RCV002429345
dbSNP Id: rs121913309
COSMIC: COSM962 COSM985
MyVariant Identifiers: chr10:g.43615613_43615624del (hg19) chr10:g.43120165_43120176del (hg38)
PubMed: PMID:25157968
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43120167_43120178del , CM000672.2:g.43120167_43120178del GRCh38
NC_000010.10:g.43615615_43615626del , CM000672.1:g.43615615_43615626del GRCh37
NC_000010.9:g.42935621_42935632del NCBI36
NG_007489.1:g.48099_48110del , LRG_518:g.48099_48110del

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.2298_2309del ENSP00000480088.2:p.Asp766_Glu769del
ENST00000683007.1:n.2268_2279del
ENST00000683872.1:n.2259_2270del
ENST00000340058.6:c.2694_2705del ENSP00000344798.4:p.Asp898_Glu901del
ENST00000355710.8:c.2694_2705del MANE Select ENSP00000347942.3:p.Asp898_Glu901del
ENST00000671844.1:c.*1288_*1299del ENSP00000500541.1:n.*1288_*1299del
ENST00000672389.1:c.*1288_*1299del ENSP00000500252.1:n.*1288_*1299del
ENST00000340058.5:c.2694_2705del ENSP00000344798.4:p.Asp898_Glu901del
ENST00000355710.7:c.2694_2705del ENSP00000347942.3:p.Asp898_Glu901del
ENST00000615310.4:c.*43_*54del ENSP00000480088.1:n.*43_*54del
NM_020630.4:c.2694_2705del , LRG_518t2:c.2694_2705del NP_065681.1:p.Asp898_Glu901del
NM_020975.4:c.2694_2705del , LRG_518t1:c.2694_2705del NP_066124.1:p.Asp898_Glu901del
XM_011540027.1:c.2694_2705del XP_011538329.1:p.Asp898_Glu901del
NM_001355216.1:c.1932_1943del NP_001342145.1:p.Asp644_Glu647del
NM_020630.5:c.2694_2705del NP_065681.1:p.Asp898_Glu901del
NM_020975.5:c.2694_2705del NP_066124.1:p.Asp898_Glu901del
NM_020975.6:c.2694_2705del MANE Select NP_066124.1:p.Asp898_Glu901del
NM_020630.6:c.2694_2705del NP_065681.1:p.Asp898_Glu901del
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