Canonical Allele Identifier: CA2608897182
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130252A>G , CM000672.2:g.43130252A>G GRCh38
NC_000010.10:g.43625700A>G , CM000672.1:g.43625700A>G GRCh37
NC_000010.9:g.42945706A>G NCBI36
NG_007489.1:g.58184A>G , LRG_518:g.58184A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3498A>G ENSP00000480088.2:n.*3498A>G
ENST00000683007.1:n.6291A>G
ENST00000355710.8:c.*1983A>G MANE Select ENSP00000347942.3:n.*1983A>G
ENST00000355710.7:c.*1983A>G ENSP00000347942.3:n.*1983A>G
ENST00000615310.4:c.*2677A>G ENSP00000480088.1:n.*2677A>G
NM_020975.4:c.*1983A>G , LRG_518t1:c.*1983A>G NP_066124.1:n.*1983A>G
XM_011540027.1:c.*751A>G XP_011538329.1:n.*751A>G
NM_020975.5:c.*1983A>G NP_066124.1:n.*1983A>G
NM_020975.6:c.*1983A>G MANE Select NP_066124.1:n.*1983A>G