Canonical Allele Identifier: CA927682499
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838418206

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130280A>T , CM000672.2:g.43130280A>T GRCh38
NC_000010.10:g.43625728A>T , CM000672.1:g.43625728A>T GRCh37
NC_000010.9:g.42945734A>T NCBI36
NG_007489.1:g.58212A>T , LRG_518:g.58212A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2011A>T MANE Select ENSP00000347942.3:n.*2011A>T
ENST00000355710.7:c.*2011A>T ENSP00000347942.3:n.*2011A>T
ENST00000615310.4:c.*2705A>T ENSP00000480088.1:n.*2705A>T
NM_020975.4:c.*2011A>T , LRG_518t1:c.*2011A>T NP_066124.1:n.*2011A>T
XM_011540027.1:c.*779A>T XP_011538329.1:n.*779A>T
NM_020975.5:c.*2011A>T NP_066124.1:n.*2011A>T
NM_020975.6:c.*2011A>T MANE Select NP_066124.1:n.*2011A>T