Canonical Allele Identifier: CA007804

Gene: RET

Linked Data

• ClinVar Variation Id: 13944
• ClinVar RCV Id: RCV000014971 ; RCV000414355 ; RCV000736274 ; RCV001013275 ; RCV001851862
• dbSNP Id: rs77558292
• MyVariant Identifiers: chr10:g.43609069T>C (hg19) ; chr10:g.43113621T>C (hg38)
• PubMed: PMID:8 ; PMID:157 ; PMID:338 ; PMID:390 ; PMID:711 ; PMID:807 ; PMID:8807338 ; PMID:10982477

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113621T>C , CM000672.2:g.43113621T>C	GRCh38
NC_000010.10:g.43609069T>C , CM000672.1:g.43609069T>C	GRCh37
NC_000010.9:g.42929075T>C	NCBI36
NG_007489.1:g.41553T>C , LRG_518:g.41553T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1429T>C	ENSP00000480088.2:p.Cys477Arg
ENST00000683007.1:n.1399T>C
ENST00000683872.1:n.586T>C
ENST00000340058.6:c.1825T>C	ENSP00000344798.4:p.Cys609Arg
ENST00000355710.8:c.1825T>C MANE Select	ENSP00000347942.3:p.Cys609Arg
ENST00000671844.1:c.*419T>C	ENSP00000500541.1:n.*419T>C
ENST00000672389.1:c.*419T>C	ENSP00000500252.1:n.*419T>C
ENST00000340058.5:c.1825T>C	ENSP00000344798.4:p.Cys609Arg
ENST00000355710.7:c.1825T>C	ENSP00000347942.3:p.Cys609Arg
ENST00000498820.5:c.376T>C	ENSP00000419080.1:p.Cys126Arg
ENST00000615310.4:c.1289+2389T>C	ENSP00000480088.1:n.1289+2389T>C
NM_020630.4:c.1825T>C , LRG_518t2:c.1825T>C	NP_065681.1:p.Cys609Arg
NM_020975.4:c.1825T>C , LRG_518t1:c.1825T>C	NP_066124.1:p.Cys609Arg
XM_011540027.1:c.1825T>C	XP_011538329.1:p.Cys609Arg
NM_001355216.1:c.1063T>C	NP_001342145.1:p.Cys355Arg
NM_020630.5:c.1825T>C	NP_065681.1:p.Cys609Arg
NM_020975.5:c.1825T>C	NP_066124.1:p.Cys609Arg
NM_020975.6:c.1825T>C MANE Select	NP_066124.1:p.Cys609Arg
NM_020630.6:c.1825T>C	NP_065681.1:p.Cys609Arg