Canonical Allele Identifier: CA927684896
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077064G>C , CM000672.2:g.43077064G>C GRCh38
NC_000010.10:g.43572512G>C , CM000672.1:g.43572512G>C GRCh37
NC_000010.9:g.42892518G>C NCBI36
NG_007489.1:g.4996G>C , LRG_518:g.4996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000671844.1:c.-195G>C ENSP00000500541.1:n.-195G>C
ENST00000355710.7:c.-195G>C ENSP00000347942.3:n.-195G>C
XM_011540027.1:c.-195G>C XP_011538329.1:n.-195G>C
NM_020630.5:c.-195G>C NP_065681.1:n.-195G>C
NM_020975.5:c.-195G>C NP_066124.1:n.-195G>C