Canonical Allele Identifier: CA1905814001
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077068C= , CM000672.2:g.43077068C= GRCh38
NC_000010.10:g.43572516C= , CM000672.1:g.43572516C= GRCh37
NC_000010.9:g.42892522C= NCBI36
NG_007489.1:g.5000C= , LRG_518:g.5000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000671844.1:c.-191C= ENSP00000500541.1:n.-191C=
ENST00000355710.7:c.-191C= ENSP00000347942.3:n.-191C=
XM_011540027.1:c.-191C= XP_011538329.1:n.-191C=
NM_020630.5:c.-191C= NP_065681.1:n.-191C=
NM_020975.5:c.-191C= NP_066124.1:n.-191C=