Canonical Allele Identifier: CA658761132
Gene: RET HGNC NCBI

Linked Data

PubMed: PMID:85 PMID:499 PMID:572 PMID:583 PMID:824
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113653_43113654delinsTC , CM000672.2:g.43113653_43113654delinsTC GRCh38
NC_000010.10:g.43609101_43609102delinsTC , CM000672.1:g.43609101_43609102delinsTC GRCh37
NC_000010.9:g.42929107_42929108delinsTC NCBI36
NG_007489.1:g.41585_41586delinsTC , LRG_518:g.41585_41586delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1461_1462delinsTC ENSP00000480088.2:p.Cys488Arg
ENST00000683007.1:n.1431_1432delinsTC
ENST00000683872.1:n.618_619delinsTC
ENST00000340058.6:c.1857_1858delinsTC ENSP00000344798.4:p.Cys620Arg
ENST00000355710.8:c.1857_1858delinsTC MANE Select ENSP00000347942.3:p.Cys620Arg
ENST00000671844.1:c.*451_*452delinsTC ENSP00000500541.1:n.*451_*452delinsTC
ENST00000672389.1:c.*451_*452delinsTC ENSP00000500252.1:n.*451_*452delinsTC
ENST00000340058.5:c.1857_1858delinsTC ENSP00000344798.4:p.Cys620Arg
ENST00000355710.7:c.1857_1858delinsTC ENSP00000347942.3:p.Cys620Arg
ENST00000498820.5:c.408_409delinsTC ENSP00000419080.1:p.Cys137Arg
ENST00000615310.4:c.1289+2421_1289+2422delinsTC ENSP00000480088.1:n.1289+2421_1289+2422de...
NM_020630.4:c.1857_1858delinsTC , LRG_518t2:c.1857_1858delinsTC NP_065681.1:p.Cys620Arg
NM_020975.4:c.1857_1858delinsTC , LRG_518t1:c.1857_1858delinsTC NP_066124.1:p.Cys620Arg
XM_011540027.1:c.1857_1858delinsTC XP_011538329.1:p.Cys620Arg
NM_001355216.1:c.1095_1096delinsTC NP_001342145.1:p.Cys366Arg
NM_020630.5:c.1857_1858delinsTC NP_065681.1:p.Cys620Arg
NM_020975.5:c.1857_1858delinsTC NP_066124.1:p.Cys620Arg
NM_020975.6:c.1857_1858delinsTC MANE Select NP_066124.1:p.Cys620Arg
NM_020630.6:c.1857_1858delinsTC NP_065681.1:p.Cys620Arg
Search 100 bp 5'
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