Canonical Allele Identifier: CA2573145094
Community Standard Title: NM_020975.6(RET):c.3188-15T>A
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43128097T>A , CM000672.2:g.43128097T>A GRCh38
NC_000010.10:g.43623545T>A , CM000672.1:g.43623545T>A GRCh37
NC_000010.9:g.42943551T>A NCBI36
NG_007489.1:g.56029T>A , LRG_518:g.56029T>A

Transcript Alleles

HGVS Amino-acid Change
NM_020975.6:c.3188-15T>A MANE Select NP_066124.1:n.3188-15T>A
ENST00000355710.8:c.3188-15T>A MANE Select ENSP00000347942.3:n.3188-15T>A
NM_020975.4:c.3188-15T>A , LRG_518t1:c.3188-15T>A NP_066124.1:n.3188-15T>A
NM_020975.5:c.3188-15T>A NP_066124.1:n.3188-15T>A
ENST00000355710.7:c.3188-15T>A ENSP00000347942.3:n.3188-15T>A
ENST00000615310.4:c.*537-15T>A ENSP00000480088.1:n.*537-15T>A
ENST00000615310.5:c.*1343T>A ENSP00000480088.2:n.*1343T>A
ENST00000683007.1:n.4136T>A
XM_011540027.1:c.3188-15T>A XP_011538329.1:n.3188-15T>A