Canonical Allele Identifier: CA376556801

Gene: RET

Linked Data

• ClinVar Variation Id: 665292
• ClinVar RCV Id: RCV000823545 ; RCV002434025
• dbSNP Id: rs1334494092
• gnomAD v2: 10-43615182-G-A
• gnomAD v4: 10-43119734-G-A
• MyVariant Identifiers: chr10:g.43615182G>A (hg19) ; chr10:g.43119734G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119734G>A , CM000672.2:g.43119734G>A	GRCh38
NC_000010.10:g.43615182G>A , CM000672.1:g.43615182G>A	GRCh37
NC_000010.9:g.42935188G>A	NCBI36
NG_007489.1:g.47666G>A , LRG_518:g.47666G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2200G>A	ENSP00000480088.2:p.Ala734Thr
ENST00000683007.1:n.2170G>A
ENST00000683872.1:n.2161G>A
ENST00000340058.6:c.2596G>A	ENSP00000344798.4:p.Ala866Thr
ENST00000355710.8:c.2596G>A MANE Select	ENSP00000347942.3:p.Ala866Thr
ENST00000671844.1:c.*1190G>A	ENSP00000500541.1:n.*1190G>A
ENST00000672389.1:c.*1190G>A	ENSP00000500252.1:n.*1190G>A
ENST00000340058.5:c.2596G>A	ENSP00000344798.4:p.Ala866Thr
ENST00000355710.7:c.2596G>A	ENSP00000347942.3:p.Ala866Thr
ENST00000615310.4:c.1322G>A	ENSP00000480088.1:p.Gly441Asp
NM_020630.4:c.2596G>A , LRG_518t2:c.2596G>A	NP_065681.1:p.Ala866Thr
NM_020975.4:c.2596G>A , LRG_518t1:c.2596G>A	NP_066124.1:p.Ala866Thr
XM_011540027.1:c.2596G>A	XP_011538329.1:p.Ala866Thr
NM_001355216.1:c.1834G>A	NP_001342145.1:p.Ala612Thr
NM_020630.5:c.2596G>A	NP_065681.1:p.Ala866Thr
NM_020975.5:c.2596G>A	NP_066124.1:p.Ala866Thr
NM_020975.6:c.2596G>A MANE Select	NP_066124.1:p.Ala866Thr
NM_020630.6:c.2596G>A	NP_065681.1:p.Ala866Thr