Canonical Allele Identifier: CA128327
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1897685
ClinVar RCV Id: RCV002572537
dbSNP Id: rs377767440
MyVariant Identifiers: chr10:g.43610046delinsTTCT (hg19) chr10:g.43114598delinsTTCT (hg38)
PubMed: PMID:158 PMID:447 PMID:681 PMID:862 PMID:894 PMID:15844786
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114598delinsTTCT , CM000672.2:g.43114598delinsTTCT GRCh38
NC_000010.10:g.43610046delinsTTCT , CM000672.1:g.43610046delinsTTCT GRCh37
NC_000010.9:g.42930052delinsTTCT NCBI36
NG_007489.1:g.42530delinsTTCT , LRG_518:g.42530delinsTTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1602delinsTTCT ENSP00000480088.2:p.Lys534delinsAsnSer
ENST00000683007.1:n.1572delinsTTCT
ENST00000683872.1:n.1563delinsTTCT
ENST00000340058.6:c.1998delinsTTCT ENSP00000344798.4:p.Lys666delinsAsnSer
ENST00000355710.8:c.1998delinsTTCT MANE Select ENSP00000347942.3:p.Lys666delinsAsnSer
ENST00000671844.1:c.*592delinsTTCT ENSP00000500541.1:n.*592delinsTTCT
ENST00000672389.1:c.*592delinsTTCT ENSP00000500252.1:n.*592delinsTTCT
ENST00000340058.5:c.1998delinsTTCT ENSP00000344798.4:p.Lys666delinsAsnSer
ENST00000355710.7:c.1998delinsTTCT ENSP00000347942.3:p.Lys666delinsAsnSer
ENST00000615310.4:c.1289+3366delinsTTCT ENSP00000480088.1:n.1289+3366delinsTTCT
NM_020630.4:c.1998delinsTTCT , LRG_518t2:c.1998delinsTTCT NP_065681.1:p.Lys666delinsAsnSer
NM_020975.4:c.1998delinsTTCT , LRG_518t1:c.1998delinsTTCT NP_066124.1:p.Lys666delinsAsnSer
XM_011540027.1:c.1998delinsTTCT XP_011538329.1:p.Lys666delinsAsnSer
NM_001355216.1:c.1236delinsTTCT NP_001342145.1:p.Lys412delinsAsnSer
NM_020630.5:c.1998delinsTTCT NP_065681.1:p.Lys666delinsAsnSer
NM_020975.5:c.1998delinsTTCT NP_066124.1:p.Lys666delinsAsnSer
NM_020975.6:c.1998delinsTTCT MANE Select NP_066124.1:p.Lys666delinsAsnSer
NM_020630.6:c.1998delinsTTCT NP_065681.1:p.Lys666delinsAsnSer
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