Canonical Allele Identifier: CA2608894557
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077330del , CM000672.2:g.43077330del GRCh38
NC_000010.10:g.43572778del , CM000672.1:g.43572778del GRCh37
NC_000010.9:g.42892784del NCBI36
NG_007489.1:g.5262del , LRG_518:g.5262del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.72del ENSP00000480088.2:p.Val25TrpfsTer?
ENST00000340058.6:c.72del ENSP00000344798.4:p.Val25TrpfsTer?
ENST00000355710.8:c.72del MANE Select ENSP00000347942.3:p.Val25TrpfsTer?
ENST00000671844.1:c.72del ENSP00000500541.1:p.Val25TrpfsTer?
ENST00000672389.1:c.72del ENSP00000500252.1:p.Asp25IlefsTer?
ENST00000340058.5:c.72del ENSP00000344798.4:p.Val25TrpfsTer?
ENST00000355710.7:c.72del ENSP00000347942.3:p.Val25TrpfsTer?
ENST00000498820.5:c.72del ENSP00000419080.1:p.Asp25MetfsTer?
ENST00000615310.4:c.72del ENSP00000480088.1:p.Val25TrpfsTer?
NM_020630.4:c.72del , LRG_518t2:c.72del NP_065681.1:p.Val25TrpfsTer?
NM_020975.4:c.72del , LRG_518t1:c.72del NP_066124.1:p.Val25TrpfsTer?
XM_011540027.1:c.72del XP_011538329.1:p.Val25TrpfsTer?
NM_020630.5:c.72del NP_065681.1:p.Val25TrpfsTer?
NM_020975.5:c.72del NP_066124.1:p.Val25TrpfsTer?
NM_020975.6:c.72del MANE Select NP_066124.1:p.Val25TrpfsTer?
NM_020630.6:c.72del NP_065681.1:p.Val25TrpfsTer?