Canonical Allele Identifier: CA2608897173
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43130199-TTAAG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130202_43130205del , CM000672.2:g.43130202_43130205del GRCh38
NC_000010.10:g.43625650_43625653del , CM000672.1:g.43625650_43625653del GRCh37
NC_000010.9:g.42945656_42945659del NCBI36
NG_007489.1:g.58134_58137del , LRG_518:g.58134_58137del

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3448_*3451del ENSP00000480088.2:n.*3448_*3451del
ENST00000683007.1:n.6241_6244del
ENST00000355710.8:c.*1933_*1936del MANE Select ENSP00000347942.3:n.*1933_*1936del
ENST00000355710.7:c.*1933_*1936del ENSP00000347942.3:n.*1933_*1936del
ENST00000615310.4:c.*2627_*2630del ENSP00000480088.1:n.*2627_*2630del
NM_020975.4:c.*1933_*1936del , LRG_518t1:c.*1933_*1936del NP_066124.1:n.*1933_*1936del
XM_011540027.1:c.*701_*704del XP_011538329.1:n.*701_*704del
NM_020975.5:c.*1933_*1936del NP_066124.1:n.*1933_*1936del
NM_020975.6:c.*1933_*1936del MANE Select NP_066124.1:n.*1933_*1936del
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