Canonical Allele Identifier: CA1905813991
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077058T= , CM000672.2:g.43077058T= GRCh38
NC_000010.10:g.43572506T= , CM000672.1:g.43572506T= GRCh37
NC_000010.9:g.42892512T= NCBI36
NG_007489.1:g.4990T= , LRG_518:g.4990T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-201T= ENSP00000347942.3:n.-201T=
XM_011540027.1:c.-201T= XP_011538329.1:n.-201T=
NM_020630.5:c.-201T= NP_065681.1:n.-201T=
NM_020975.5:c.-201T= NP_066124.1:n.-201T=