Canonical Allele Identifier: CA008926

Gene: RET

Linked Data

• ClinVar Variation Id: 194425
• ClinVar RCV Id: RCV000174791
• dbSNP Id: rs794727130
• MyVariant Identifiers: chr10:g.43615172_43615178del (hg19) ; chr10:g.43119724_43119730del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119724_43119730del , CM000672.2:g.43119724_43119730del	GRCh38
NC_000010.10:g.43615172_43615178del , CM000672.1:g.43615172_43615178del	GRCh37
NC_000010.9:g.42935178_42935184del	NCBI36
NG_007489.1:g.47656_47662del , LRG_518:g.47656_47662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2190_2196del	ENSP00000480088.2:p.Met730IlefsTer5
ENST00000683007.1:n.2160_2166del
ENST00000683872.1:n.2151_2157del
ENST00000340058.6:c.2586_2592del	ENSP00000344798.4:p.Met862IlefsTer5
ENST00000355710.8:c.2586_2592del MANE Select	ENSP00000347942.3:p.Met862IlefsTer5
ENST00000671844.1:c.*1180_*1186del	ENSP00000500541.1:n.*1180_*1186del
ENST00000672389.1:c.*1180_*1186del	ENSP00000500252.1:n.*1180_*1186del
ENST00000340058.5:c.2586_2592del	ENSP00000344798.4:p.Met862IlefsTer5
ENST00000355710.7:c.2586_2592del	ENSP00000347942.3:p.Met862IlefsTer5
ENST00000615310.4:c.1312_1318del	ENSP00000480088.1:p.Ala438LeufsTer?
NM_020630.4:c.2586_2592del , LRG_518t2:c.2586_2592del	NP_065681.1:p.Met862IlefsTer5
NM_020975.4:c.2586_2592del , LRG_518t1:c.2586_2592del	NP_066124.1:p.Met862IlefsTer5
XM_011540027.1:c.2586_2592del	XP_011538329.1:p.Met862IlefsTer5
NM_001355216.1:c.1824_1830del	NP_001342145.1:p.Met608IlefsTer5
NM_020630.5:c.2586_2592del	NP_065681.1:p.Met862IlefsTer5
NM_020975.5:c.2586_2592del	NP_066124.1:p.Met862IlefsTer5
NM_020975.6:c.2586_2592del MANE Select	NP_066124.1:p.Met862IlefsTer5
NM_020630.6:c.2586_2592del	NP_065681.1:p.Met862IlefsTer5