Canonical Allele Identifier: CA1905833034
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130254_43130258delinsCTATT , CM000672.2:g.43130254_43130258delinsCTATT GRCh38
NC_000010.10:g.43625702_43625706delinsCTATT , CM000672.1:g.43625702_43625706delinsCTATT GRCh37
NC_000010.9:g.42945708_42945712delinsCTATT NCBI36
NG_007489.1:g.58186_58190delinsCTATT , LRG_518:g.58186_58190delinsCTATT

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3500_*3504delinsCTATT ENSP00000480088.2:n.*3500_*3504delinsCTAT...
ENST00000683007.1:n.6293_6297delinsCTATT
ENST00000355710.8:c.*1985_*1989delinsCTATT MANE Select ENSP00000347942.3:n.*1985_*1989delinsCTAT...
ENST00000355710.7:c.*1985_*1989delinsCTATT ENSP00000347942.3:n.*1985_*1989delinsCTAT...
ENST00000615310.4:c.*2679_*2683delinsCTATT ENSP00000480088.1:n.*2679_*2683delinsCTAT...
NM_020975.4:c.*1985_*1989delinsCTATT , LRG_518t1:c.*1985_*1989delinsCTATT NP_066124.1:n.*1985_*1989delinsCTATT
XM_011540027.1:c.*753_*757delinsCTATT XP_011538329.1:n.*753_*757delinsCTATT
NM_020975.5:c.*1985_*1989delinsCTATT NP_066124.1:n.*1985_*1989delinsCTATT
NM_020975.6:c.*1985_*1989delinsCTATT MANE Select NP_066124.1:n.*1985_*1989delinsCTATT