Canonical Allele Identifier: CA007883

Gene: RET

Linked Data

• ClinVar Variation Id: 24897
• ClinVar RCV Id: RCV000506649
• dbSNP Id: rs377767391
• MyVariant Identifiers: chr10:g.43609075T>G (hg19) ; chr10:g.43113627T>G (hg38)
• PubMed: PMID:73 ; PMID:511 ; PMID:534 ; PMID:706 ; PMID:967 ; PMID:9677065

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113627T>G , CM000672.2:g.43113627T>G	GRCh38
NC_000010.10:g.43609075T>G , CM000672.1:g.43609075T>G	GRCh37
NC_000010.9:g.42929081T>G	NCBI36
NG_007489.1:g.41559T>G , LRG_518:g.41559T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1435T>G	ENSP00000480088.2:p.Cys479Gly
ENST00000683007.1:n.1405T>G
ENST00000683872.1:n.592T>G
ENST00000340058.6:c.1831T>G	ENSP00000344798.4:p.Cys611Gly
ENST00000355710.8:c.1831T>G MANE Select	ENSP00000347942.3:p.Cys611Gly
ENST00000671844.1:c.*425T>G	ENSP00000500541.1:n.*425T>G
ENST00000672389.1:c.*425T>G	ENSP00000500252.1:n.*425T>G
ENST00000340058.5:c.1831T>G	ENSP00000344798.4:p.Cys611Gly
ENST00000355710.7:c.1831T>G	ENSP00000347942.3:p.Cys611Gly
ENST00000498820.5:c.382T>G	ENSP00000419080.1:p.Cys128Gly
ENST00000615310.4:c.1289+2395T>G	ENSP00000480088.1:n.1289+2395T>G
NM_020630.4:c.1831T>G , LRG_518t2:c.1831T>G	NP_065681.1:p.Cys611Gly
NM_020975.4:c.1831T>G , LRG_518t1:c.1831T>G	NP_066124.1:p.Cys611Gly
XM_011540027.1:c.1831T>G	XP_011538329.1:p.Cys611Gly
NM_001355216.1:c.1069T>G	NP_001342145.1:p.Cys357Gly
NM_020630.5:c.1831T>G	NP_065681.1:p.Cys611Gly
NM_020975.5:c.1831T>G	NP_066124.1:p.Cys611Gly
NM_020975.6:c.1831T>G MANE Select	NP_066124.1:p.Cys611Gly
NM_020630.6:c.1831T>G	NP_065681.1:p.Cys611Gly