Canonical Allele Identifier: CA2740092981

Gene: RET

Linked Data

• ClinVar Variation Id: 3061203
• ClinVar RCV Id: RCV003982715

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114571_43114578del , CM000672.2:g.43114571_43114578del	GRCh38
NC_000010.10:g.43610019_43610026del , CM000672.1:g.43610019_43610026del	GRCh37
NC_000010.9:g.42930025_42930032del	NCBI36
NG_007489.1:g.42503_42510del , LRG_518:g.42503_42510del

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1575_1582del	ENSP00000480088.2:p.His526ProfsTer13
ENST00000683007.1:n.1545_1552del
ENST00000683872.1:n.1536_1543del
ENST00000340058.6:c.1971_1978del	ENSP00000344798.4:p.His658ProfsTer13
ENST00000355710.8:c.1971_1978del MANE Select	ENSP00000347942.3:p.His658ProfsTer13
ENST00000671844.1:c.*565_*572del	ENSP00000500541.1:n.*565_*572del
ENST00000672389.1:c.*565_*572del	ENSP00000500252.1:n.*565_*572del
ENST00000340058.5:c.1971_1978del	ENSP00000344798.4:p.His658ProfsTer13
ENST00000355710.7:c.1971_1978del	ENSP00000347942.3:p.His658ProfsTer13
ENST00000498820.5:c.522_529del	ENSP00000419080.1:p.His175ProfsTer?
ENST00000615310.4:c.1289+3339_1289+3346del	ENSP00000480088.1:n.1289+3339_1289+3346del
NM_020630.4:c.1971_1978del , LRG_518t2:c.1971_1978del	NP_065681.1:p.His658ProfsTer13
NM_020975.4:c.1971_1978del , LRG_518t1:c.1971_1978del	NP_066124.1:p.His658ProfsTer13
XM_011540027.1:c.1971_1978del	XP_011538329.1:p.His658ProfsTer13
NM_001355216.1:c.1209_1216del	NP_001342145.1:p.His404ProfsTer13
NM_020630.5:c.1971_1978del	NP_065681.1:p.His658ProfsTer13
NM_020975.5:c.1971_1978del	NP_066124.1:p.His658ProfsTer13
NM_020975.6:c.1971_1978del MANE Select	NP_066124.1:p.His658ProfsTer13
NM_020630.6:c.1971_1978del	NP_065681.1:p.His658ProfsTer13