Canonical Allele Identifier: CA1905813995
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077063_43077066dup , CM000672.2:g.43077063_43077066dup GRCh38
NC_000010.10:g.43572511_43572514dup , CM000672.1:g.43572511_43572514dup GRCh37
NC_000010.9:g.42892517_42892520dup NCBI36
NG_007489.1:g.4995_4998dup , LRG_518:g.4995_4998dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-196_-193dup ENSP00000347942.3:n.-196_-193dup
XM_011540027.1:c.-196_-193dup XP_011538329.1:n.-196_-193dup
NM_020630.5:c.-196_-193dup NP_065681.1:n.-196_-193dup
NM_020975.5:c.-196_-193dup NP_066124.1:n.-196_-193dup