Canonical Allele Identifier: CA665316483

Gene: RET

Linked Data

• ClinVar Variation Id: 879101
• ClinVar RCV Id: RCV001106292 ; RCV001106293 ; RCV001106290 ; RCV001106291
• dbSNP Id: rs1353594500
• gnomAD v3: 10-43129381-A-G
• gnomAD v4: 10-43129381-A-G
• MyVariant Identifiers: chr10:g.43624829A>G (hg19) ; chr10:g.43129381A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43129381A>G , CM000672.2:g.43129381A>G	GRCh38
NC_000010.10:g.43624829A>G , CM000672.1:g.43624829A>G	GRCh37
NC_000010.9:g.42944835A>G	NCBI36
NG_007489.1:g.57313A>G , LRG_518:g.57313A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*2627A>G	ENSP00000480088.2:n.*2627A>G
ENST00000683007.1:n.5420A>G
ENST00000355710.8:c.*1112A>G MANE Select	ENSP00000347942.3:n.*1112A>G
ENST00000355710.7:c.*1112A>G	ENSP00000347942.3:n.*1112A>G
ENST00000615310.4:c.*1806A>G	ENSP00000480088.1:n.*1806A>G
NM_020975.4:c.*1112A>G , LRG_518t1:c.*1112A>G	NP_066124.1:n.*1112A>G
XM_011540027.1:c.*17-137A>G	XP_011538329.1:n.*17-137A>G
NM_020975.5:c.*1112A>G	NP_066124.1:n.*1112A>G
NM_020975.6:c.*1112A>G MANE Select	NP_066124.1:n.*1112A>G