Canonical Allele Identifier: CA2580081458

Gene: RET

Linked Data

• ClinVar Variation Id: 1737851
• ClinVar RCV Id: RCV002323341

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077299_43077301delinsGGTTGCTGC , CM000672.2:g.43077299_43077301delinsGGTTGCTGC	GRCh38
NC_000010.10:g.43572747_43572749delinsGGTTGCTGC , CM000672.1:g.43572747_43572749delinsGGTTGCTGC	GRCh37
NC_000010.9:g.42892753_42892755delinsGGTTGCTGC	NCBI36
NG_007489.1:g.5231_5233delinsGGTTGCTGC , LRG_518:g.5231_5233delinsGGTTGCTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.41_43delinsGGTTGCTGC	ENSP00000480088.2:p.Leu13_Leu14insArgLeu
ENST00000340058.6:c.41_43delinsGGTTGCTGC	ENSP00000344798.4:p.Leu13_Leu14insArgLeu
ENST00000355710.8:c.41_43delinsGGTTGCTGC MANE Select	ENSP00000347942.3:p.Leu13_Leu14insArgLeu
ENST00000671844.1:c.41_43delinsGGTTGCTGC	ENSP00000500541.1:p.Leu13_Leu14insArgLeu
ENST00000672389.1:c.41_43delinsGGTTGCTGC	ENSP00000500252.1:p.Leu13_Leu14insArgLeu
ENST00000340058.5:c.41_43delinsGGTTGCTGC	ENSP00000344798.4:p.Leu13_Leu14insArgLeu
ENST00000355710.7:c.41_43delinsGGTTGCTGC	ENSP00000347942.3:p.Leu13_Leu14insArgLeu
ENST00000498820.5:c.41_43delinsGGTTGCTGC	ENSP00000419080.1:p.Leu13_Leu14insArgLeu
ENST00000615310.4:c.41_43delinsGGTTGCTGC	ENSP00000480088.1:p.Leu13_Leu14insArgLeu
NM_020630.4:c.41_43delinsGGTTGCTGC , LRG_518t2:c.41_43delinsGGTTGCTGC	NP_065681.1:p.Leu13_Leu14insArgLeu
NM_020975.4:c.41_43delinsGGTTGCTGC , LRG_518t1:c.41_43delinsGGTTGCTGC	NP_066124.1:p.Leu13_Leu14insArgLeu
XM_011540027.1:c.41_43delinsGGTTGCTGC	XP_011538329.1:p.Leu13_Leu14insArgLeu
NM_020630.5:c.41_43delinsGGTTGCTGC	NP_065681.1:p.Leu13_Leu14insArgLeu
NM_020975.5:c.41_43delinsGGTTGCTGC	NP_066124.1:p.Leu13_Leu14insArgLeu
NM_020975.6:c.41_43delinsGGTTGCTGC MANE Select	NP_066124.1:p.Leu13_Leu14insArgLeu
NM_020630.6:c.41_43delinsGGTTGCTGC	NP_065681.1:p.Leu13_Leu14insArgLeu