Canonical Allele Identifier: CA891842881

Gene: RET

Linked Data

• ClinVar Variation Id: 580433
• ClinVar RCV Id: RCV000703975 ; RCV002332497
• dbSNP Id: rs1488217326
• MyVariant Identifiers: chr10:g.43572749_43572757del (hg19) ; chr10:g.43077301_43077309del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077301_43077309del , CM000672.2:g.43077301_43077309del	GRCh38
NC_000010.10:g.43572749_43572757del , CM000672.1:g.43572749_43572757del	GRCh37
NC_000010.9:g.42892755_42892763del	NCBI36
NG_007489.1:g.5233_5241del , LRG_518:g.5233_5241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.43_51del	ENSP00000480088.2:p.Leu15_Leu17del
ENST00000340058.6:c.43_51del	ENSP00000344798.4:p.Leu15_Leu17del
ENST00000355710.8:c.43_51del MANE Select	ENSP00000347942.3:p.Leu15_Leu17del
ENST00000671844.1:c.43_51del	ENSP00000500541.1:p.Leu15_Leu17del
ENST00000672389.1:c.43_51del	ENSP00000500252.1:p.Leu15_Leu17del
ENST00000340058.5:c.43_51del	ENSP00000344798.4:p.Leu15_Leu17del
ENST00000355710.7:c.43_51del	ENSP00000347942.3:p.Leu15_Leu17del
ENST00000498820.5:c.43_51del	ENSP00000419080.1:p.Leu15_Leu17del
ENST00000615310.4:c.43_51del	ENSP00000480088.1:p.Leu15_Leu17del
NM_020630.4:c.43_51del , LRG_518t2:c.43_51del	NP_065681.1:p.Leu15_Leu17del
NM_020975.4:c.43_51del , LRG_518t1:c.43_51del	NP_066124.1:p.Leu15_Leu17del
XM_011540027.1:c.43_51del	XP_011538329.1:p.Leu15_Leu17del
NM_020630.5:c.43_51del	NP_065681.1:p.Leu15_Leu17del
NM_020975.5:c.43_51del	NP_066124.1:p.Leu15_Leu17del
NM_020975.6:c.43_51del MANE Select	NP_066124.1:p.Leu15_Leu17del
NM_020630.6:c.43_51del	NP_065681.1:p.Leu15_Leu17del