Canonical Allele Identifier: CA927682443
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1838417421
gnomAD v3: 10-43130245-T-C
gnomAD v4: 10-43130245-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130245T>C , CM000672.2:g.43130245T>C GRCh38
NC_000010.10:g.43625693T>C , CM000672.1:g.43625693T>C GRCh37
NC_000010.9:g.42945699T>C NCBI36
NG_007489.1:g.58177T>C , LRG_518:g.58177T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3491T>C ENSP00000480088.2:n.*3491T>C
ENST00000683007.1:n.6284T>C
ENST00000355710.8:c.*1976T>C MANE Select ENSP00000347942.3:n.*1976T>C
ENST00000355710.7:c.*1976T>C ENSP00000347942.3:n.*1976T>C
ENST00000615310.4:c.*2670T>C ENSP00000480088.1:n.*2670T>C
NM_020975.4:c.*1976T>C , LRG_518t1:c.*1976T>C NP_066124.1:n.*1976T>C
XM_011540027.1:c.*744T>C XP_011538329.1:n.*744T>C
NM_020975.5:c.*1976T>C NP_066124.1:n.*1976T>C
NM_020975.6:c.*1976T>C MANE Select NP_066124.1:n.*1976T>C
Search 100 bp 5'
Search 100 bp 3'