Canonical Allele Identifier: CA009216
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136117
dbSNP Id: rs587780812

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077289C>G , CM000672.2:g.43077289C>G GRCh38
NC_000010.10:g.43572737C>G , CM000672.1:g.43572737C>G GRCh37
NC_000010.9:g.42892743C>G NCBI36
NG_007489.1:g.5221C>G , LRG_518:g.5221C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.31C>G ENSP00000480088.2:p.Leu11Val
ENST00000340058.6:c.31C>G ENSP00000344798.4:p.Leu11Val
ENST00000355710.8:c.31C>G MANE Select ENSP00000347942.3:p.Leu11Val
ENST00000671844.1:c.31C>G ENSP00000500541.1:p.Leu11Val
ENST00000672389.1:c.31C>G ENSP00000500252.1:p.Leu11Val
ENST00000340058.5:c.31C>G ENSP00000344798.4:p.Leu11Val
ENST00000355710.7:c.31C>G ENSP00000347942.3:p.Leu11Val
ENST00000498820.5:c.31C>G ENSP00000419080.1:p.Leu11Val
ENST00000615310.4:c.31C>G ENSP00000480088.1:p.Leu11Val
NM_020630.4:c.31C>G , LRG_518t2:c.31C>G NP_065681.1:p.Leu11Val
NM_020975.4:c.31C>G , LRG_518t1:c.31C>G NP_066124.1:p.Leu11Val
XM_011540027.1:c.31C>G XP_011538329.1:p.Leu11Val
NM_020630.5:c.31C>G NP_065681.1:p.Leu11Val
NM_020975.5:c.31C>G NP_066124.1:p.Leu11Val
NM_020975.6:c.31C>G MANE Select NP_066124.1:p.Leu11Val
NM_020630.6:c.31C>G NP_065681.1:p.Leu11Val