Canonical Allele Identifier: CA658761132

Gene: RET

Linked Data

• PubMed: PMID:85 ; PMID:499 ; PMID:572 ; PMID:583 ; PMID:824

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113653_43113654delinsTC , CM000672.2:g.43113653_43113654delinsTC	GRCh38
NC_000010.10:g.43609101_43609102delinsTC , CM000672.1:g.43609101_43609102delinsTC	GRCh37
NC_000010.9:g.42929107_42929108delinsTC	NCBI36
NG_007489.1:g.41585_41586delinsTC , LRG_518:g.41585_41586delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1461_1462delinsTC	ENSP00000480088.2:p.Cys488Arg
ENST00000683007.1:n.1431_1432delinsTC
ENST00000683872.1:n.618_619delinsTC
ENST00000340058.6:c.1857_1858delinsTC	ENSP00000344798.4:p.Cys620Arg
ENST00000355710.8:c.1857_1858delinsTC MANE Select	ENSP00000347942.3:p.Cys620Arg
ENST00000671844.1:c.*451_*452delinsTC	ENSP00000500541.1:n.*451_*452delinsTC
ENST00000672389.1:c.*451_*452delinsTC	ENSP00000500252.1:n.*451_*452delinsTC
ENST00000340058.5:c.1857_1858delinsTC	ENSP00000344798.4:p.Cys620Arg
ENST00000355710.7:c.1857_1858delinsTC	ENSP00000347942.3:p.Cys620Arg
ENST00000498820.5:c.408_409delinsTC	ENSP00000419080.1:p.Cys137Arg
ENST00000615310.4:c.1289+2421_1289+2422delinsTC	ENSP00000480088.1:n.1289+2421_1289+2422delinsTC
NM_020630.4:c.1857_1858delinsTC , LRG_518t2:c.1857_1858delinsTC	NP_065681.1:p.Cys620Arg
NM_020975.4:c.1857_1858delinsTC , LRG_518t1:c.1857_1858delinsTC	NP_066124.1:p.Cys620Arg
XM_011540027.1:c.1857_1858delinsTC	XP_011538329.1:p.Cys620Arg
NM_001355216.1:c.1095_1096delinsTC	NP_001342145.1:p.Cys366Arg
NM_020630.5:c.1857_1858delinsTC	NP_065681.1:p.Cys620Arg
NM_020975.5:c.1857_1858delinsTC	NP_066124.1:p.Cys620Arg
NM_020975.6:c.1857_1858delinsTC MANE Select	NP_066124.1:p.Cys620Arg
NM_020630.6:c.1857_1858delinsTC	NP_065681.1:p.Cys620Arg