Canonical Allele Identifier: CA1905814000
Gene: RET HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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