Canonical Allele Identifier: CA10628580

Gene: RET

Linked Data

• ClinVar Variation Id: 299941
• ClinVar RCV Id: RCV000282802 ; RCV000322689 ; RCV000347551 ; RCV000377190
• dbSNP Id: rs886047012
• gnomAD v3: 10-43129928-T-C
• gnomAD v4: 10-43129928-T-C
• MyVariant Identifiers: chr10:g.43625376T>C (hg19) ; chr10:g.43129928T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43129928T>C , CM000672.2:g.43129928T>C	GRCh38
NC_000010.10:g.43625376T>C , CM000672.1:g.43625376T>C	GRCh37
NC_000010.9:g.42945382T>C	NCBI36
NG_007489.1:g.57860T>C , LRG_518:g.57860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3174T>C	ENSP00000480088.2:n.*3174T>C
ENST00000683007.1:n.5967T>C
ENST00000355710.8:c.*1659T>C MANE Select	ENSP00000347942.3:n.*1659T>C
ENST00000355710.7:c.*1659T>C	ENSP00000347942.3:n.*1659T>C
ENST00000615310.4:c.*2353T>C	ENSP00000480088.1:n.*2353T>C
NM_020975.4:c.*1659T>C , LRG_518t1:c.*1659T>C	NP_066124.1:n.*1659T>C
XM_011540027.1:c.*427T>C	XP_011538329.1:n.*427T>C
NM_020975.5:c.*1659T>C	NP_066124.1:n.*1659T>C
NM_020975.6:c.*1659T>C MANE Select	NP_066124.1:n.*1659T>C