Canonical Allele Identifier: CA1905813971
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077038C= , CM000672.2:g.43077038C= GRCh38
NC_000010.10:g.43572486C= , CM000672.1:g.43572486C= GRCh37
NC_000010.9:g.42892492C= NCBI36
NG_007489.1:g.4970C= , LRG_518:g.4970C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355710.7:c.-221C= ENSP00000347942.3:n.-221C=
XM_011540027.1:c.-221C= XP_011538329.1:n.-221C=
NM_020630.5:c.-221C= NP_065681.1:n.-221C=
NM_020975.5:c.-221C= NP_066124.1:n.-221C=