Canonical Allele Identifier: CA1905833047
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130272_43130273delinsTA , CM000672.2:g.43130272_43130273delinsTA GRCh38
NC_000010.10:g.43625720_43625721delinsTA , CM000672.1:g.43625720_43625721delinsTA GRCh37
NC_000010.9:g.42945726_42945727delinsTA NCBI36
NG_007489.1:g.58204_58205delinsTA , LRG_518:g.58204_58205delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2003_*2004delinsTA MANE Select ENSP00000347942.3:n.*2003_*2004delinsTA
ENST00000355710.7:c.*2003_*2004delinsTA ENSP00000347942.3:n.*2003_*2004delinsTA
ENST00000615310.4:c.*2697_*2698delinsTA ENSP00000480088.1:n.*2697_*2698delinsTA
NM_020975.4:c.*2003_*2004delinsTA , LRG_518t1:c.*2003_*2004delinsTA NP_066124.1:n.*2003_*2004delinsTA
XM_011540027.1:c.*771_*772delinsTA XP_011538329.1:n.*771_*772delinsTA
NM_020975.5:c.*2003_*2004delinsTA NP_066124.1:n.*2003_*2004delinsTA
NM_020975.6:c.*2003_*2004delinsTA MANE Select NP_066124.1:n.*2003_*2004delinsTA