Canonical Allele Identifier: CA007792

Gene: RET

Linked Data

• dbSNP Id: rs77558292
• MyVariant Identifiers: chr10:g.43609069T>A (hg19) ; chr10:g.43113621T>A (hg38)
• PubMed: PMID:1 ; PMID:195 ; PMID:326 ; PMID:553 ; PMID:630 ; PMID:915 ; PMID:11955539

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1429T>A	ENSP00000480088.2:p.Cys477Ser
ENST00000683007.1:n.1399T>A
ENST00000683872.1:n.586T>A
ENST00000340058.6:c.1825T>A	ENSP00000344798.4:p.Cys609Ser
ENST00000355710.8:c.1825T>A MANE Select	ENSP00000347942.3:p.Cys609Ser
ENST00000671844.1:c.*419T>A	ENSP00000500541.1:n.*419T>A
ENST00000672389.1:c.*419T>A	ENSP00000500252.1:n.*419T>A
ENST00000340058.5:c.1825T>A	ENSP00000344798.4:p.Cys609Ser
ENST00000355710.7:c.1825T>A	ENSP00000347942.3:p.Cys609Ser
ENST00000498820.5:c.376T>A	ENSP00000419080.1:p.Cys126Ser
ENST00000615310.4:c.1289+2389T>A	ENSP00000480088.1:n.1289+2389T>A
NM_020630.4:c.1825T>A , LRG_518t2:c.1825T>A	NP_065681.1:p.Cys609Ser
NM_020975.4:c.1825T>A , LRG_518t1:c.1825T>A	NP_066124.1:p.Cys609Ser
XM_011540027.1:c.1825T>A	XP_011538329.1:p.Cys609Ser
NM_001355216.1:c.1063T>A	NP_001342145.1:p.Cys355Ser
NM_020630.5:c.1825T>A	NP_065681.1:p.Cys609Ser
NM_020975.5:c.1825T>A	NP_066124.1:p.Cys609Ser
NM_020975.6:c.1825T>A MANE Select	NP_066124.1:p.Cys609Ser
NM_020630.6:c.1825T>A	NP_065681.1:p.Cys609Ser