Canonical Allele Identifier: CA2608894107
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077088_43077099del , CM000672.2:g.43077088_43077099del GRCh38
NC_000010.10:g.43572536_43572547del , CM000672.1:g.43572536_43572547del GRCh37
NC_000010.9:g.42892542_42892553del NCBI36
NG_007489.1:g.5020_5031del , LRG_518:g.5020_5031del

Transcript Alleles

HGVS Amino-acid change
ENST00000340058.6:c.-171_-160del ENSP00000344798.4:n.-171_-160del
ENST00000355710.8:c.-171_-160del MANE Select ENSP00000347942.3:n.-171_-160del
ENST00000671844.1:c.-171_-160del ENSP00000500541.1:n.-171_-160del
ENST00000672389.1:c.-171_-160del ENSP00000500252.1:n.-171_-160del
ENST00000340058.5:c.-171_-160del ENSP00000344798.4:n.-171_-160del
ENST00000355710.7:c.-171_-160del ENSP00000347942.3:n.-171_-160del
ENST00000498820.5:c.-171_-160del ENSP00000419080.1:n.-171_-160del
ENST00000615310.4:c.-171_-160del ENSP00000480088.1:n.-171_-160del
NM_020630.4:c.-171_-160del , LRG_518t2:c.-171_-160del NP_065681.1:n.-171_-160del
NM_020975.4:c.-171_-160del , LRG_518t1:c.-171_-160del NP_066124.1:n.-171_-160del
XM_011540027.1:c.-171_-160del XP_011538329.1:n.-171_-160del
NM_020630.5:c.-171_-160del NP_065681.1:n.-171_-160del
NM_020975.5:c.-171_-160del NP_066124.1:n.-171_-160del
NM_020975.6:c.-171_-160del MANE Select NP_066124.1:n.-171_-160del
NM_020630.6:c.-171_-160del NP_065681.1:n.-171_-160del