Canonical Allele Identifier: CA645541247

Gene: RET

Linked Data

• COSMIC: COSM27040

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114486_43114491del , CM000672.2:g.43114486_43114491del	GRCh38
NC_000010.10:g.43609934_43609939del , CM000672.1:g.43609934_43609939del	GRCh37
NC_000010.9:g.42929940_42929945del	NCBI36
NG_007489.1:g.42418_42423del , LRG_518:g.42418_42423del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1490_1495del	ENSP00000480088.2:p.Leu497_Asp499delinsHis
ENST00000683007.1:n.1460_1465del
ENST00000683872.1:n.1451_1456del
ENST00000340058.6:c.1886_1891del	ENSP00000344798.4:p.Leu629_Asp631delinsHis
ENST00000355710.8:c.1886_1891del MANE Select	ENSP00000347942.3:p.Leu629_Asp631delinsHis
ENST00000671844.1:c.*480_*485del	ENSP00000500541.1:n.*480_*485del
ENST00000672389.1:c.*480_*485del	ENSP00000500252.1:n.*480_*485del
ENST00000340058.5:c.1886_1891del	ENSP00000344798.4:p.Leu629_Asp631delinsHis
ENST00000355710.7:c.1886_1891del	ENSP00000347942.3:p.Leu629_Asp631delinsHis
ENST00000498820.5:c.437_442del	ENSP00000419080.1:p.Leu146_Asp148delinsHis
ENST00000615310.4:c.1289+3254_1289+3259del	ENSP00000480088.1:n.1289+3254_1289+3259del
NM_020630.4:c.1886_1891del , LRG_518t2:c.1886_1891del	NP_065681.1:p.Leu629_Asp631delinsHis
NM_020975.4:c.1886_1891del , LRG_518t1:c.1886_1891del	NP_066124.1:p.Leu629_Asp631delinsHis
XM_011540027.1:c.1886_1891del	XP_011538329.1:p.Leu629_Asp631delinsHis
NM_001355216.1:c.1124_1129del	NP_001342145.1:p.Leu375_Asp377delinsHis
NM_020630.5:c.1886_1891del	NP_065681.1:p.Leu629_Asp631delinsHis
NM_020975.5:c.1886_1891del	NP_066124.1:p.Leu629_Asp631delinsHis
NM_020975.6:c.1886_1891del MANE Select	NP_066124.1:p.Leu629_Asp631delinsHis
NM_020630.6:c.1886_1891del	NP_065681.1:p.Leu629_Asp631delinsHis