Canonical Allele Identifier: CA008989
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13951
dbSNP Id: rs75234356

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43120144T>G , CM000672.2:g.43120144T>G GRCh38
NC_000010.10:g.43615592T>G , CM000672.1:g.43615592T>G GRCh37
NC_000010.9:g.42935598T>G NCBI36
NG_007489.1:g.48076T>G , LRG_518:g.48076T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.2275T>G ENSP00000480088.2:p.Ser759Ala
ENST00000683007.1:n.2245T>G
ENST00000683872.1:n.2236T>G
ENST00000340058.6:c.2671T>G ENSP00000344798.4:p.Ser891Ala
ENST00000355710.8:c.2671T>G MANE Select ENSP00000347942.3:p.Ser891Ala
ENST00000671844.1:c.*1265T>G ENSP00000500541.1:n.*1265T>G
ENST00000672389.1:c.*1265T>G ENSP00000500252.1:n.*1265T>G
ENST00000340058.5:c.2671T>G ENSP00000344798.4:p.Ser891Ala
ENST00000355710.7:c.2671T>G ENSP00000347942.3:p.Ser891Ala
ENST00000615310.4:c.*20T>G ENSP00000480088.1:n.*20T>G
NM_020630.4:c.2671T>G , LRG_518t2:c.2671T>G NP_065681.1:p.Ser891Ala
NM_020975.4:c.2671T>G , LRG_518t1:c.2671T>G NP_066124.1:p.Ser891Ala
XM_011540027.1:c.2671T>G XP_011538329.1:p.Ser891Ala
NM_001355216.1:c.1909T>G NP_001342145.1:p.Ser637Ala
NM_020630.5:c.2671T>G NP_065681.1:p.Ser891Ala
NM_020975.5:c.2671T>G NP_066124.1:p.Ser891Ala
NM_020975.6:c.2671T>G MANE Select NP_066124.1:p.Ser891Ala
NM_020630.6:c.2671T>G NP_065681.1:p.Ser891Ala