Canonical Allele Identifier: CA10582718

Gene: RET

Linked Data

• ClinVar Variation Id: 241364
• ClinVar RCV Id: RCV000225980 ; RCV002347912
• dbSNP Id: rs878855065
• gnomAD v4: 10-43077308-T-TGCTGCTGCC
• MyVariant Identifiers: chr10:g.43572763_43572771dupGCCGCTGCT (hg19) ; chr10:g.43572756_43572757insGCTGCTGCC (hg19) ; chr10:g.43077315_43077323dupGCCGCTGCT (hg38) ; chr10:g.43077308_43077309insGCTGCTGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077315_43077323dup , CM000672.2:g.43077315_43077323dup	GRCh38
NC_000010.10:g.43572763_43572771dup , CM000672.1:g.43572763_43572771dup	GRCh37
NC_000010.9:g.42892769_42892777dup	NCBI36
NG_007489.1:g.5247_5255dup , LRG_518:g.5247_5255dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.57_65dup	ENSP00000480088.2:p.Leu22_Gly23insProLeuLeu
ENST00000340058.6:c.57_65dup	ENSP00000344798.4:p.Leu22_Gly23insProLeuLeu
ENST00000355710.8:c.57_65dup MANE Select	ENSP00000347942.3:p.Leu22_Gly23insProLeuLeu
ENST00000671844.1:c.57_65dup	ENSP00000500541.1:p.Leu22_Gly23insProLeuLeu
ENST00000672389.1:c.57_65dup	ENSP00000500252.1:p.Leu22_Gly23insProLeuLeu
ENST00000340058.5:c.57_65dup	ENSP00000344798.4:p.Leu22_Gly23insProLeuLeu
ENST00000355710.7:c.57_65dup	ENSP00000347942.3:p.Leu22_Gly23insProLeuLeu
ENST00000498820.5:c.57_65dup	ENSP00000419080.1:p.Leu22_Gly23insProLeuLeu
ENST00000615310.4:c.57_65dup	ENSP00000480088.1:p.Leu22_Gly23insProLeuLeu
NM_020630.4:c.57_65dup , LRG_518t2:c.57_65dup	NP_065681.1:p.Leu22_Gly23insProLeuLeu
NM_020975.4:c.57_65dup , LRG_518t1:c.57_65dup	NP_066124.1:p.Leu22_Gly23insProLeuLeu
XM_011540027.1:c.57_65dup	XP_011538329.1:p.Leu22_Gly23insProLeuLeu
NM_020630.5:c.57_65dup	NP_065681.1:p.Leu22_Gly23insProLeuLeu
NM_020975.5:c.57_65dup	NP_066124.1:p.Leu22_Gly23insProLeuLeu
NM_020975.6:c.57_65dup MANE Select	NP_066124.1:p.Leu22_Gly23insProLeuLeu
NM_020630.6:c.57_65dup	NP_065681.1:p.Leu22_Gly23insProLeuLeu