Canonical Allele Identifier: CA916081576

Gene: RET

Linked Data

• ClinVar Variation Id: 835920
• ClinVar RCV Id: RCV001036920 ; RCV002346246
• dbSNP Id: rs768132465
• gnomAD v4: 10-43077301-TTGCTGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077311_43077316del , CM000672.2:g.43077311_43077316del	GRCh38
NC_000010.10:g.43572759_43572764del , CM000672.1:g.43572759_43572764del	GRCh37
NC_000010.9:g.42892765_42892770del	NCBI36
NG_007489.1:g.5243_5248del , LRG_518:g.5243_5248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.53_58del	ENSP00000480088.2:p.Leu18_Leu19del
ENST00000340058.6:c.53_58del	ENSP00000344798.4:p.Leu18_Leu19del
ENST00000355710.8:c.53_58del MANE Select	ENSP00000347942.3:p.Leu18_Leu19del
ENST00000671844.1:c.53_58del	ENSP00000500541.1:p.Leu18_Leu19del
ENST00000672389.1:c.53_58del	ENSP00000500252.1:p.Leu18_Leu19del
ENST00000340058.5:c.53_58del	ENSP00000344798.4:p.Leu18_Leu19del
ENST00000355710.7:c.53_58del	ENSP00000347942.3:p.Leu18_Leu19del
ENST00000498820.5:c.53_58del	ENSP00000419080.1:p.Leu18_Leu19del
ENST00000615310.4:c.53_58del	ENSP00000480088.1:p.Leu18_Leu19del
NM_020630.4:c.53_58del , LRG_518t2:c.53_58del	NP_065681.1:p.Leu18_Leu19del
NM_020975.4:c.53_58del , LRG_518t1:c.53_58del	NP_066124.1:p.Leu18_Leu19del
XM_011540027.1:c.53_58del	XP_011538329.1:p.Leu18_Leu19del
NM_020630.5:c.53_58del	NP_065681.1:p.Leu18_Leu19del
NM_020975.5:c.53_58del	NP_066124.1:p.Leu18_Leu19del
NM_020975.6:c.53_58del MANE Select	NP_066124.1:p.Leu18_Leu19del
NM_020630.6:c.53_58del	NP_065681.1:p.Leu18_Leu19del