Canonical Allele Identifier: CA008271

Gene: RET

Linked Data

• dbSNP Id: rs377767408
• MyVariant Identifiers: chr10:g.43609944_43609948delinsCGTGC (hg19) ; chr10:g.43114496_43114500delinsCGTGC (hg38)
• PubMed: PMID:124 ; PMID:286 ; PMID:797 ; PMID:809 ; PMID:920 ; PMID:8099202

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114496_43114500delinsCGTGC , CM000672.2:g.43114496_43114500delinsCGTGC	GRCh38
NC_000010.10:g.43609944_43609948delinsCGTGC , CM000672.1:g.43609944_43609948delinsCGTGC	GRCh37
NC_000010.9:g.42929950_42929954delinsCGTGC	NCBI36
NG_007489.1:g.42428_42432delinsCGTGC , LRG_518:g.42428_42432delinsCGTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1500_1504delinsCGTGC	ENSP00000480088.2:p.Glu500_Cys502delinsAspValArg
ENST00000683007.1:n.1470_1474delinsCGTGC
ENST00000683872.1:n.1461_1465delinsCGTGC
ENST00000340058.6:c.1896_1900delinsCGTGC	ENSP00000344798.4:p.Glu632_Cys634delinsAspValArg
ENST00000355710.8:c.1896_1900delinsCGTGC MANE Select	ENSP00000347942.3:p.Glu632_Cys634delinsAspValArg
ENST00000671844.1:c.*490_*494delinsCGTGC	ENSP00000500541.1:n.*490_*494delinsCGTGC
ENST00000672389.1:c.*490_*494delinsCGTGC	ENSP00000500252.1:n.*490_*494delinsCGTGC
ENST00000340058.5:c.1896_1900delinsCGTGC	ENSP00000344798.4:p.Glu632_Cys634delinsAspValArg
ENST00000355710.7:c.1896_1900delinsCGTGC	ENSP00000347942.3:p.Glu632_Cys634delinsAspValArg
ENST00000498820.5:c.447_451delinsCGTGC	ENSP00000419080.1:p.Glu149_Cys151delinsAspValArg
ENST00000615310.4:c.1289+3264_1289+3268delinsCGTGC	ENSP00000480088.1:n.1289+3264_1289+3268delinsCGTGC
NM_020630.4:c.1896_1900delinsCGTGC , LRG_518t2:c.1896_1900delinsCGTGC	NP_065681.1:p.Glu632_Cys634delinsAspValArg
NM_020975.4:c.1896_1900delinsCGTGC , LRG_518t1:c.1896_1900delinsCGTGC	NP_066124.1:p.Glu632_Cys634delinsAspValArg
XM_011540027.1:c.1896_1900delinsCGTGC	XP_011538329.1:p.Glu632_Cys634delinsAspValArg
NM_001355216.1:c.1134_1138delinsCGTGC	NP_001342145.1:p.Glu378_Cys380delinsAspValArg
NM_020630.5:c.1896_1900delinsCGTGC	NP_065681.1:p.Glu632_Cys634delinsAspValArg
NM_020975.5:c.1896_1900delinsCGTGC	NP_066124.1:p.Glu632_Cys634delinsAspValArg
NM_020975.6:c.1896_1900delinsCGTGC MANE Select	NP_066124.1:p.Glu632_Cys634delinsAspValArg
NM_020630.6:c.1896_1900delinsCGTGC	NP_065681.1:p.Glu632_Cys634delinsAspValArg