Canonical Allele Identifier: CA038434
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486317
dbSNP Id: rs748799148

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43118378G>A , CM000672.2:g.43118378G>A GRCh38
NC_000010.10:g.43613826G>A , CM000672.1:g.43613826G>A GRCh37
NC_000010.9:g.42933832G>A NCBI36
NG_007489.1:g.46310G>A , LRG_518:g.46310G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1894G>A ENSP00000480088.2:p.Ala632Thr
ENST00000683007.1:n.1864G>A
ENST00000683872.1:n.1855G>A
ENST00000340058.6:c.2290G>A ENSP00000344798.4:p.Ala764Thr
ENST00000355710.8:c.2290G>A MANE Select ENSP00000347942.3:p.Ala764Thr
ENST00000671844.1:c.*884G>A ENSP00000500541.1:n.*884G>A
ENST00000672389.1:c.*884G>A ENSP00000500252.1:n.*884G>A
ENST00000340058.5:c.2290G>A ENSP00000344798.4:p.Ala764Thr
ENST00000355710.7:c.2290G>A ENSP00000347942.3:p.Ala764Thr
ENST00000615310.4:c.1290-1324G>A ENSP00000480088.1:n.1290-1324G>A
NM_020630.4:c.2290G>A , LRG_518t2:c.2290G>A NP_065681.1:p.Ala764Thr
NM_020975.4:c.2290G>A , LRG_518t1:c.2290G>A NP_066124.1:p.Ala764Thr
XM_011540027.1:c.2290G>A XP_011538329.1:p.Ala764Thr
NM_001355216.1:c.1528G>A NP_001342145.1:p.Ala510Thr
NM_020630.5:c.2290G>A NP_065681.1:p.Ala764Thr
NM_020975.5:c.2290G>A NP_066124.1:p.Ala764Thr
NM_020975.6:c.2290G>A MANE Select NP_066124.1:p.Ala764Thr
NM_020630.6:c.2290G>A NP_065681.1:p.Ala764Thr