Canonical Allele Identifier: CA009374
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24880
dbSNP Id: rs34682185

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43106382G>A , CM000672.2:g.43106382G>A GRCh38
NC_000010.10:g.43601830G>A , CM000672.1:g.43601830G>A GRCh37
NC_000010.9:g.42921836G>A NCBI36
NG_007489.1:g.34314G>A , LRG_518:g.34314G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.867+1189G>A ENSP00000480088.2:p.=
ENST00000683007.1:n.448G>A
ENST00000340058.6:c.874G>A ENSP00000344798.4:p.Val292Met
ENST00000355710.8:c.874G>A MANE Select ENSP00000347942.3:p.Val292Met
ENST00000671844.1:c.625+3753G>A ENSP00000500541.1:p.=
ENST00000672389.1:c.74-4825G>A ENSP00000500252.1:p.=
ENST00000340058.5:c.874G>A ENSP00000344798.4:p.Val292Met
ENST00000355710.7:c.874G>A ENSP00000347942.3:p.Val292Met
ENST00000479913.1:n.469G>A
ENST00000498820.5:c.74-5717G>A ENSP00000419080.1:p.=
ENST00000615310.4:c.874G>A ENSP00000480088.1:p.Val292Met
NM_020630.4:c.874G>A , LRG_518t2:c.874G>A NP_065681.1:p.Val292Met
NM_020975.4:c.874G>A , LRG_518t1:c.874G>A NP_066124.1:p.Val292Met
XM_011540027.1:c.874G>A XP_011538329.1:p.Val292Met
NM_001355216.1:c.112G>A NP_001342145.1:p.Val38Met
NM_020630.5:c.874G>A NP_065681.1:p.Val292Met
NM_020975.5:c.874G>A NP_066124.1:p.Val292Met
NM_020975.6:c.874G>A MANE Select NP_066124.1:p.Val292Met
NM_020630.6:c.874G>A NP_065681.1:p.Val292Met