Canonical Allele Identifier: CA2573053272

Gene: RET

Linked Data

• ClinVar Variation Id: 1338394
• ClinVar RCV Id: RCV001817765
• dbSNP Id: rs2132844768

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114502_43114503delinsTT , CM000672.2:g.43114502_43114503delinsTT	GRCh38
NC_000010.10:g.43609950_43609951delinsTT , CM000672.1:g.43609950_43609951delinsTT	GRCh37
NC_000010.9:g.42929956_42929957delinsTT	NCBI36
NG_007489.1:g.42434_42435delinsTT , LRG_518:g.42434_42435delinsTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1506_1507delinsTT	ENSP00000480088.2:p.Arg503Cys
ENST00000683007.1:n.1476_1477delinsTT
ENST00000683872.1:n.1467_1468delinsTT
ENST00000340058.6:c.1902_1903delinsTT	ENSP00000344798.4:p.Arg635Cys
ENST00000355710.8:c.1902_1903delinsTT MANE Select	ENSP00000347942.3:p.Arg635Cys
ENST00000671844.1:c.*496_*497delinsTT	ENSP00000500541.1:n.*496_*497delinsTT
ENST00000672389.1:c.*496_*497delinsTT	ENSP00000500252.1:n.*496_*497delinsTT
ENST00000340058.5:c.1902_1903delinsTT	ENSP00000344798.4:p.Arg635Cys
ENST00000355710.7:c.1902_1903delinsTT	ENSP00000347942.3:p.Arg635Cys
ENST00000498820.5:c.453_454delinsTT	ENSP00000419080.1:p.Arg152Cys
ENST00000615310.4:c.1289+3270_1289+3271delinsTT	ENSP00000480088.1:n.1289+3270_1289+3271de...
NM_020630.4:c.1902_1903delinsTT , LRG_518t2:c.1902_1903delinsTT	NP_065681.1:p.Arg635Cys
NM_020975.4:c.1902_1903delinsTT , LRG_518t1:c.1902_1903delinsTT	NP_066124.1:p.Arg635Cys
XM_011540027.1:c.1902_1903delinsTT	XP_011538329.1:p.Arg635Cys
NM_001355216.1:c.1140_1141delinsTT	NP_001342145.1:p.Arg381Cys
NM_020630.5:c.1902_1903delinsTT	NP_065681.1:p.Arg635Cys
NM_020975.5:c.1902_1903delinsTT	NP_066124.1:p.Arg635Cys
NM_020975.6:c.1902_1903delinsTT MANE Select	NP_066124.1:p.Arg635Cys
NM_020630.6:c.1902_1903delinsTT	NP_065681.1:p.Arg635Cys