Canonical Allele Identifier: CA1905813998
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077062_43077079delinsTCGCTTCAGTCCCGCGAC , CM000672.2:g.43077062_43077079delinsTCGCTTCAGTCCCGCGAC GRCh38
NC_000010.10:g.43572510_43572527delinsTCGCTTCAGTCCCGCGAC , CM000672.1:g.43572510_43572527delinsTCGCTTCAGTCCCGCGAC GRCh37
NC_000010.9:g.42892516_42892533delinsTCGCTTCAGTCCCGCGAC NCBI36
NG_007489.1:g.4994_5011delinsTCGCTTCAGTCCCGCGAC , LRG_518:g.4994_5011delinsTCGCTTCAGTCCCGCGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-197_-180delinsTCGCTTCAGTCCCGCGAC ENSP00000347942.3:n.-197_-180delinsTCGCTTCAGTCCCGCGAC
XM_011540027.1:c.-197_-180delinsTCGCTTCAGTCCCGCGAC XP_011538329.1:n.-197_-180delinsTCGCTTCAGTCCCGCGAC
NM_020630.5:c.-197_-180delinsTCGCTTCAGTCCCGCGAC NP_065681.1:n.-197_-180delinsTCGCTTCAGTCCCGCGAC
NM_020975.5:c.-197_-180delinsTCGCTTCAGTCCCGCGAC NP_066124.1:n.-197_-180delinsTCGCTTCAGTCCCGCGAC