Canonical Allele Identifier: CA008013
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13914
dbSNP Id: rs79781594

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43113649G>C , CM000672.2:g.43113649G>C GRCh38
NC_000010.10:g.43609097G>C , CM000672.1:g.43609097G>C GRCh37
NC_000010.9:g.42929103G>C NCBI36
NG_007489.1:g.41581G>C , LRG_518:g.41581G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1457G>C ENSP00000480088.2:p.Cys486Ser
ENST00000683007.1:n.1427G>C
ENST00000683872.1:n.614G>C
ENST00000340058.6:c.1853G>C ENSP00000344798.4:p.Cys618Ser
ENST00000355710.8:c.1853G>C MANE Select ENSP00000347942.3:p.Cys618Ser
ENST00000671844.1:c.*447G>C ENSP00000500541.1:n.*447G>C
ENST00000672389.1:c.*447G>C ENSP00000500252.1:n.*447G>C
ENST00000340058.5:c.1853G>C ENSP00000344798.4:p.Cys618Ser
ENST00000355710.7:c.1853G>C ENSP00000347942.3:p.Cys618Ser
ENST00000498820.5:c.404G>C ENSP00000419080.1:p.Cys135Ser
ENST00000615310.4:c.1289+2417G>C ENSP00000480088.1:n.1289+2417G>C
NM_020630.4:c.1853G>C , LRG_518t2:c.1853G>C NP_065681.1:p.Cys618Ser
NM_020975.4:c.1853G>C , LRG_518t1:c.1853G>C NP_066124.1:p.Cys618Ser
XM_011540027.1:c.1853G>C XP_011538329.1:p.Cys618Ser
NM_001355216.1:c.1091G>C NP_001342145.1:p.Cys364Ser
NM_020630.5:c.1853G>C NP_065681.1:p.Cys618Ser
NM_020975.5:c.1853G>C NP_066124.1:p.Cys618Ser
NM_020975.6:c.1853G>C MANE Select NP_066124.1:p.Cys618Ser
NM_020630.6:c.1853G>C NP_065681.1:p.Cys618Ser