Canonical Allele Identifier: CA2721934393
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs2132939902

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119388A>G , CM000672.2:g.43119388A>G GRCh38
NC_000010.10:g.43614836A>G , CM000672.1:g.43614836A>G GRCh37
NC_000010.9:g.42934842A>G NCBI36
NG_007489.1:g.47320A>G , LRG_518:g.47320A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.1997-143A>G ENSP00000480088.2:n.1997-143A>G
ENST00000683007.1:n.1967-143A>G
ENST00000683872.1:n.1958-143A>G
ENST00000340058.6:c.2393-143A>G ENSP00000344798.4:n.2393-143A>G
ENST00000355710.8:c.2393-143A>G MANE Select ENSP00000347942.3:n.2393-143A>G
ENST00000671844.1:c.*987-143A>G ENSP00000500541.1:n.*987-143A>G
ENST00000672389.1:c.*987-143A>G ENSP00000500252.1:n.*987-143A>G
ENST00000340058.5:c.2393-143A>G ENSP00000344798.4:n.2393-143A>G
ENST00000355710.7:c.2393-143A>G ENSP00000347942.3:n.2393-143A>G
ENST00000615310.4:c.1290-314A>G ENSP00000480088.1:n.1290-314A>G
NM_020630.4:c.2393-143A>G , LRG_518t2:c.2393-143A>G NP_065681.1:n.2393-143A>G
NM_020975.4:c.2393-143A>G , LRG_518t1:c.2393-143A>G NP_066124.1:n.2393-143A>G
XM_011540027.1:c.2393-143A>G XP_011538329.1:n.2393-143A>G
NM_001355216.1:c.1631-143A>G NP_001342145.1:n.1631-143A>G
NM_020630.5:c.2393-143A>G NP_065681.1:n.2393-143A>G
NM_020975.5:c.2393-143A>G NP_066124.1:n.2393-143A>G
NM_020975.6:c.2393-143A>G MANE Select NP_066124.1:n.2393-143A>G
NM_020630.6:c.2393-143A>G NP_065681.1:n.2393-143A>G