Canonical Allele Identifier: CA1905833058
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130281T= , CM000672.2:g.43130281T= GRCh38
NC_000010.10:g.43625729T= , CM000672.1:g.43625729T= GRCh37
NC_000010.9:g.42945735T= NCBI36
NG_007489.1:g.58213T= , LRG_518:g.58213T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2012T= MANE Select ENSP00000347942.3:n.*2012T=
ENST00000355710.7:c.*2012T= ENSP00000347942.3:n.*2012T=
ENST00000615310.4:c.*2706T= ENSP00000480088.1:n.*2706T=
NM_020975.4:c.*2012T= , LRG_518t1:c.*2012T= NP_066124.1:n.*2012T=
XM_011540027.1:c.*780T= XP_011538329.1:n.*780T=
NM_020975.5:c.*2012T= NP_066124.1:n.*2012T=
NM_020975.6:c.*2012T= MANE Select NP_066124.1:n.*2012T=