Canonical Allele Identifier: CA1905833005
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130210T= , CM000672.2:g.43130210T= GRCh38
NC_000010.10:g.43625658T= , CM000672.1:g.43625658T= GRCh37
NC_000010.9:g.42945664T= NCBI36
NG_007489.1:g.58142T= , LRG_518:g.58142T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.*3456T= ENSP00000480088.2:n.*3456T=
ENST00000683007.1:n.6249T=
ENST00000355710.8:c.*1941T= MANE Select ENSP00000347942.3:n.*1941T=
ENST00000355710.7:c.*1941T= ENSP00000347942.3:n.*1941T=
ENST00000615310.4:c.*2635T= ENSP00000480088.1:n.*2635T=
NM_020975.4:c.*1941T= , LRG_518t1:c.*1941T= NP_066124.1:n.*1941T=
XM_011540027.1:c.*709T= XP_011538329.1:n.*709T=
NM_020975.5:c.*1941T= NP_066124.1:n.*1941T=
NM_020975.6:c.*1941T= MANE Select NP_066124.1:n.*1941T=