Canonical Allele Identifier: CA376552905

Gene: RET

Linked Data

• ClinVar Variation Id: 1707858
• ClinVar RCV Id: RCV002287019
• dbSNP Id: rs1335705237
• gnomAD v3: 10-43114495-A-G
• gnomAD v4: 10-43114495-A-G
• MyVariant Identifiers: chr10:g.43609943A>G (hg19) ; chr10:g.43114495A>G (hg38)
• PubMed: PMID:26497911

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114495A>G , CM000672.2:g.43114495A>G	GRCh38
NC_000010.10:g.43609943A>G , CM000672.1:g.43609943A>G	GRCh37
NC_000010.9:g.42929949A>G	NCBI36
NG_007489.1:g.42427A>G , LRG_518:g.42427A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1499A>G	ENSP00000480088.2:p.Glu500Gly
ENST00000683007.1:n.1469A>G
ENST00000683872.1:n.1460A>G
ENST00000340058.6:c.1895A>G	ENSP00000344798.4:p.Glu632Gly
ENST00000355710.8:c.1895A>G MANE Select	ENSP00000347942.3:p.Glu632Gly
ENST00000671844.1:c.*489A>G	ENSP00000500541.1:n.*489A>G
ENST00000672389.1:c.*489A>G	ENSP00000500252.1:n.*489A>G
ENST00000340058.5:c.1895A>G	ENSP00000344798.4:p.Glu632Gly
ENST00000355710.7:c.1895A>G	ENSP00000347942.3:p.Glu632Gly
ENST00000498820.5:c.446A>G	ENSP00000419080.1:p.Glu149Gly
ENST00000615310.4:c.1289+3263A>G	ENSP00000480088.1:n.1289+3263A>G
NM_020630.4:c.1895A>G , LRG_518t2:c.1895A>G	NP_065681.1:p.Glu632Gly
NM_020975.4:c.1895A>G , LRG_518t1:c.1895A>G	NP_066124.1:p.Glu632Gly
XM_011540027.1:c.1895A>G	XP_011538329.1:p.Glu632Gly
NM_001355216.1:c.1133A>G	NP_001342145.1:p.Glu378Gly
NM_020630.5:c.1895A>G	NP_065681.1:p.Glu632Gly
NM_020975.5:c.1895A>G	NP_066124.1:p.Glu632Gly
NM_020975.6:c.1895A>G MANE Select	NP_066124.1:p.Glu632Gly
NM_020630.6:c.1895A>G	NP_065681.1:p.Glu632Gly