Canonical Allele Identifier: CA206268406

Gene: RET

Linked Data

• ClinVar Variation Id: 878517
• ClinVar RCV Id: RCV001105164 ; RCV001105165 ; RCV001105162 ; RCV001105163 ; RCV002264184
• dbSNP Id: rs143948954
• gnomAD v2: 10-43624763-G-C
• gnomAD v3: 10-43129315-G-C
• gnomAD v4: 10-43129315-G-C
• MyVariant Identifiers: chr10:g.43624763G>C (hg19) ; chr10:g.43129315G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43129315G>C , CM000672.2:g.43129315G>C	GRCh38
NC_000010.10:g.43624763G>C , CM000672.1:g.43624763G>C	GRCh37
NC_000010.9:g.42944769G>C	NCBI36
NG_007489.1:g.57247G>C , LRG_518:g.57247G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*2561G>C	ENSP00000480088.2:n.*2561G>C
ENST00000683007.1:n.5354G>C
ENST00000355710.8:c.*1046G>C MANE Select	ENSP00000347942.3:n.*1046G>C
ENST00000355710.7:c.*1046G>C	ENSP00000347942.3:n.*1046G>C
ENST00000615310.4:c.*1740G>C	ENSP00000480088.1:n.*1740G>C
NM_020975.4:c.*1046G>C , LRG_518t1:c.*1046G>C	NP_066124.1:n.*1046G>C
XM_011540027.1:c.*17-203G>C	XP_011538329.1:n.*17-203G>C
NM_020975.5:c.*1046G>C	NP_066124.1:n.*1046G>C
NM_020975.6:c.*1046G>C MANE Select	NP_066124.1:n.*1046G>C