Canonical Allele Identifier: CA054706
Community Standard Title: NM_020975.6(RET):c.3188-4T>G
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43128108T>G , CM000672.2:g.43128108T>G GRCh38
NC_000010.10:g.43623556T>G , CM000672.1:g.43623556T>G GRCh37
NC_000010.9:g.42943562T>G NCBI36
NG_007489.1:g.56040T>G , LRG_518:g.56040T>G

Transcript Alleles

HGVS Amino-acid Change
NM_020975.6:c.3188-4T>G MANE Select NP_066124.1:n.3188-4T>G
ENST00000355710.8:c.3188-4T>G MANE Select ENSP00000347942.3:n.3188-4T>G
NM_020975.4:c.3188-4T>G , LRG_518t1:c.3188-4T>G NP_066124.1:n.3188-4T>G
NM_020975.5:c.3188-4T>G NP_066124.1:n.3188-4T>G
ENST00000355710.7:c.3188-4T>G ENSP00000347942.3:n.3188-4T>G
ENST00000615310.4:c.*537-4T>G ENSP00000480088.1:n.*537-4T>G
ENST00000615310.5:c.*1354T>G ENSP00000480088.2:n.*1354T>G
ENST00000683007.1:n.4147T>G
XM_011540027.1:c.3188-4T>G XP_011538329.1:n.3188-4T>G