Canonical Allele Identifier: CA1905813970
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077037T= , CM000672.2:g.43077037T= GRCh38
NC_000010.10:g.43572485T= , CM000672.1:g.43572485T= GRCh37
NC_000010.9:g.42892491T= NCBI36
NG_007489.1:g.4969T= , LRG_518:g.4969T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-222T= ENSP00000347942.3:n.-222T=
XM_011540027.1:c.-222T= XP_011538329.1:n.-222T=
NM_020630.5:c.-222T= NP_065681.1:n.-222T=
NM_020975.5:c.-222T= NP_066124.1:n.-222T=