Canonical Allele Identifier: CA008264
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs267607009

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114496_43114497delinsCG , CM000672.2:g.43114496_43114497delinsCG GRCh38
NC_000010.10:g.43609944_43609945delinsCG , CM000672.1:g.43609944_43609945delinsCG GRCh37
NC_000010.9:g.42929950_42929951delinsCG NCBI36
NG_007489.1:g.42428_42429delinsCG , LRG_518:g.42428_42429delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1500_1501delinsCG ENSP00000480088.2:p.Glu500_Leu501delinsAspVal
ENST00000683007.1:n.1470_1471delinsCG
ENST00000683872.1:n.1461_1462delinsCG
ENST00000340058.6:c.1896_1897delinsCG ENSP00000344798.4:p.Glu632_Leu633delinsAspVal
ENST00000355710.8:c.1896_1897delinsCG MANE Select ENSP00000347942.3:p.Glu632_Leu633delinsAspVal
ENST00000671844.1:c.*490_*491delinsCG ENSP00000500541.1:n.*490_*491delinsCG
ENST00000672389.1:c.*490_*491delinsCG ENSP00000500252.1:n.*490_*491delinsCG
ENST00000340058.5:c.1896_1897delinsCG ENSP00000344798.4:p.Glu632_Leu633delinsAspVal
ENST00000355710.7:c.1896_1897delinsCG ENSP00000347942.3:p.Glu632_Leu633delinsAspVal
ENST00000498820.5:c.447_448delinsCG ENSP00000419080.1:p.Glu149_Leu150delinsAspVal
ENST00000615310.4:c.1289+3264_1289+3265delinsCG ENSP00000480088.1:n.1289+3264_1289+3265delinsCG
NM_020630.4:c.1896_1897delinsCG , LRG_518t2:c.1896_1897delinsCG NP_065681.1:p.Glu632_Leu633delinsAspVal
NM_020975.4:c.1896_1897delinsCG , LRG_518t1:c.1896_1897delinsCG NP_066124.1:p.Glu632_Leu633delinsAspVal
XM_011540027.1:c.1896_1897delinsCG XP_011538329.1:p.Glu632_Leu633delinsAspVal
NM_001355216.1:c.1134_1135delinsCG NP_001342145.1:p.Glu378_Leu379delinsAspVal
NM_020630.5:c.1896_1897delinsCG NP_065681.1:p.Glu632_Leu633delinsAspVal
NM_020975.5:c.1896_1897delinsCG NP_066124.1:p.Glu632_Leu633delinsAspVal
NM_020975.6:c.1896_1897delinsCG MANE Select NP_066124.1:p.Glu632_Leu633delinsAspVal
NM_020630.6:c.1896_1897delinsCG NP_065681.1:p.Glu632_Leu633delinsAspVal