Canonical Allele Identifier: CA1905833042
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838417876

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130266G>T , CM000672.2:g.43130266G>T GRCh38
NC_000010.10:g.43625714G>T , CM000672.1:g.43625714G>T GRCh37
NC_000010.9:g.42945720G>T NCBI36
NG_007489.1:g.58198G>T , LRG_518:g.58198G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3512G>T ENSP00000480088.2:n.*3512G>T
ENST00000683007.1:n.6305G>T
ENST00000355710.8:c.*1997G>T MANE Select ENSP00000347942.3:n.*1997G>T
ENST00000355710.7:c.*1997G>T ENSP00000347942.3:n.*1997G>T
ENST00000615310.4:c.*2691G>T ENSP00000480088.1:n.*2691G>T
NM_020975.4:c.*1997G>T , LRG_518t1:c.*1997G>T NP_066124.1:n.*1997G>T
XM_011540027.1:c.*765G>T XP_011538329.1:n.*765G>T
NM_020975.5:c.*1997G>T NP_066124.1:n.*1997G>T
NM_020975.6:c.*1997G>T MANE Select NP_066124.1:n.*1997G>T