Canonical Allele Identifier: CA008085
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13943
ClinVar RCV Id: RCV000014970 RCV000021802 RCV000489707 RCV001013426
dbSNP Id: rs77503355
COSMIC: COSM29805
MyVariant Identifiers: chr10:g.43609103G>C (hg19) chr10:g.43113655G>C (hg38)
PubMed: PMID:410 PMID:529 PMID:787 PMID:818 PMID:996 PMID:7874109 PMID:10777380 PMID:11454140
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113655G>C , CM000672.2:g.43113655G>C GRCh38
NC_000010.10:g.43609103G>C , CM000672.1:g.43609103G>C GRCh37
NC_000010.9:g.42929109G>C NCBI36
NG_007489.1:g.41587G>C , LRG_518:g.41587G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1463G>C ENSP00000480088.2:p.Cys488Ser
ENST00000683007.1:n.1433G>C
ENST00000683872.1:n.620G>C
ENST00000340058.6:c.1859G>C ENSP00000344798.4:p.Cys620Ser
ENST00000355710.8:c.1859G>C MANE Select ENSP00000347942.3:p.Cys620Ser
ENST00000671844.1:c.*453G>C ENSP00000500541.1:n.*453G>C
ENST00000672389.1:c.*453G>C ENSP00000500252.1:n.*453G>C
ENST00000340058.5:c.1859G>C ENSP00000344798.4:p.Cys620Ser
ENST00000355710.7:c.1859G>C ENSP00000347942.3:p.Cys620Ser
ENST00000498820.5:c.410G>C ENSP00000419080.1:p.Cys137Ser
ENST00000615310.4:c.1289+2423G>C ENSP00000480088.1:n.1289+2423G>C
NM_020630.4:c.1859G>C , LRG_518t2:c.1859G>C NP_065681.1:p.Cys620Ser
NM_020975.4:c.1859G>C , LRG_518t1:c.1859G>C NP_066124.1:p.Cys620Ser
XM_011540027.1:c.1859G>C XP_011538329.1:p.Cys620Ser
NM_001355216.1:c.1097G>C NP_001342145.1:p.Cys366Ser
NM_020630.5:c.1859G>C NP_065681.1:p.Cys620Ser
NM_020975.5:c.1859G>C NP_066124.1:p.Cys620Ser
NM_020975.6:c.1859G>C MANE Select NP_066124.1:p.Cys620Ser
NM_020630.6:c.1859G>C NP_065681.1:p.Cys620Ser
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