Canonical Allele Identifier: CA008066

Gene: RET

Linked Data

• ClinVar Variation Id: 24905
• ClinVar RCV Id: RCV000507202 ; RCV000575015 ; RCV000709757 ; RCV000824755 ; RCV001703419 ; RCV002513160
• dbSNP Id: rs77316810
• MyVariant Identifiers: chr10:g.43609102T>G (hg19) ; chr10:g.43113654T>G (hg38)
• PubMed: PMID:234 ; PMID:367 ; PMID:520 ; PMID:922 ; PMID:979 ; PMID:8918855 ; PMID:9067749 ; PMID:9223675 ; PMID:11073534 ; PMID:11502806 ; PMID:14718397 ; PMID:20979234 ; PMID:24972642 ; PMID:25694125

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113654T>G , CM000672.2:g.43113654T>G	GRCh38
NC_000010.10:g.43609102T>G , CM000672.1:g.43609102T>G	GRCh37
NC_000010.9:g.42929108T>G	NCBI36
NG_007489.1:g.41586T>G , LRG_518:g.41586T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1462T>G	ENSP00000480088.2:p.Cys488Gly
ENST00000683007.1:n.1432T>G
ENST00000683872.1:n.619T>G
ENST00000340058.6:c.1858T>G	ENSP00000344798.4:p.Cys620Gly
ENST00000355710.8:c.1858T>G MANE Select	ENSP00000347942.3:p.Cys620Gly
ENST00000671844.1:c.*452T>G	ENSP00000500541.1:n.*452T>G
ENST00000672389.1:c.*452T>G	ENSP00000500252.1:n.*452T>G
ENST00000340058.5:c.1858T>G	ENSP00000344798.4:p.Cys620Gly
ENST00000355710.7:c.1858T>G	ENSP00000347942.3:p.Cys620Gly
ENST00000498820.5:c.409T>G	ENSP00000419080.1:p.Cys137Gly
ENST00000615310.4:c.1289+2422T>G	ENSP00000480088.1:n.1289+2422T>G
NM_020630.4:c.1858T>G , LRG_518t2:c.1858T>G	NP_065681.1:p.Cys620Gly
NM_020975.4:c.1858T>G , LRG_518t1:c.1858T>G	NP_066124.1:p.Cys620Gly
XM_011540027.1:c.1858T>G	XP_011538329.1:p.Cys620Gly
NM_001355216.1:c.1096T>G	NP_001342145.1:p.Cys366Gly
NM_020630.5:c.1858T>G	NP_065681.1:p.Cys620Gly
NM_020975.5:c.1858T>G	NP_066124.1:p.Cys620Gly
NM_020975.6:c.1858T>G MANE Select	NP_066124.1:p.Cys620Gly
NM_020630.6:c.1858T>G	NP_065681.1:p.Cys620Gly