Canonical Allele Identifier: CA1905814148

Gene: RET

Linked Data

• ClinVar Variation Id: 1020843
• ClinVar RCV Id: RCV001320496 ; RCV002350589 ; RCV003321826
• dbSNP Id: rs1837063549
• gnomAD v4: 10-43077260-T-TGGCGAAGGCGACGTCCGGTGCCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077263_43077286dup , CM000672.2:g.43077263_43077286dup	GRCh38
NC_000010.10:g.43572711_43572734dup , CM000672.1:g.43572711_43572734dup	GRCh37
NC_000010.9:g.42892717_42892740dup	NCBI36
NG_007489.1:g.5195_5218dup , LRG_518:g.5195_5218dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.5_28dup	ENSP00000480088.2:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000340058.6:c.5_28dup	ENSP00000344798.4:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000355710.8:c.5_28dup MANE Select	ENSP00000347942.3:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000671844.1:c.5_28dup	ENSP00000500541.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000672389.1:c.5_28dup	ENSP00000500252.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000340058.5:c.5_28dup	ENSP00000344798.4:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000355710.7:c.5_28dup	ENSP00000347942.3:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000498820.5:c.5_28dup	ENSP00000419080.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
ENST00000615310.4:c.5_28dup	ENSP00000480088.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
NM_020630.4:c.5_28dup , LRG_518t2:c.5_28dup	NP_065681.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
NM_020975.4:c.5_28dup , LRG_518t1:c.5_28dup	NP_066124.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
XM_011540027.1:c.5_28dup	XP_011538329.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
NM_020630.5:c.5_28dup	NP_065681.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
NM_020975.5:c.5_28dup	NP_066124.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
NM_020975.6:c.5_28dup MANE Select	NP_066124.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla
NM_020630.6:c.5_28dup	NP_065681.1:p.Ala9_Gly10insAlaLysAlaThrSerGlyAlaAla