Canonical Allele Identifier: CA2838479291

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113564del , CM000672.2:g.43113564del	GRCh38
NC_000010.10:g.43609012del , CM000672.1:g.43609012del	GRCh37
NC_000010.9:g.42929018del	NCBI36
NG_007489.1:g.41496del , LRG_518:g.41496del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1372del	ENSP00000480088.2:p.Ile458LeufsTer?
ENST00000683007.1:n.1342del
ENST00000683872.1:n.529del
ENST00000340058.6:c.1768del	ENSP00000344798.4:p.Ile590LeufsTer?
ENST00000355710.8:c.1768del MANE Select	ENSP00000347942.3:p.Ile590LeufsTer?
ENST00000671844.1:c.*362del	ENSP00000500541.1:n.*362del
ENST00000672389.1:c.*362del	ENSP00000500252.1:n.*362del
ENST00000340058.5:c.1768del	ENSP00000344798.4:p.Ile590LeufsTer?
ENST00000355710.7:c.1768del	ENSP00000347942.3:p.Ile590LeufsTer?
ENST00000498820.5:c.319del	ENSP00000419080.1:p.Ile107LeufsTer?
ENST00000615310.4:c.1289+2332del	ENSP00000480088.1:n.1289+2332del
NM_020630.4:c.1768del , LRG_518t2:c.1768del	NP_065681.1:p.Ile590LeufsTer?
NM_020975.4:c.1768del , LRG_518t1:c.1768del	NP_066124.1:p.Ile590LeufsTer?
XM_011540027.1:c.1768del	XP_011538329.1:p.Ile590LeufsTer?
NM_001355216.1:c.1006del	NP_001342145.1:p.Ile336LeufsTer?
NM_020630.5:c.1768del	NP_065681.1:p.Ile590LeufsTer?
NM_020975.5:c.1768del	NP_066124.1:p.Ile590LeufsTer?
NM_020975.6:c.1768del MANE Select	NP_066124.1:p.Ile590LeufsTer?
NM_020630.6:c.1768del	NP_065681.1:p.Ile590LeufsTer?