Canonical Allele Identifier: CA10635343

Gene: RET

Linked Data

• ClinVar Variation Id: 299908
• ClinVar RCV Id: RCV000272787 ; RCV000308196 ; RCV000321083 ; RCV000365222
• dbSNP Id: rs3026782
• gnomAD v2: 10-43624105-G-A
• gnomAD v3: 10-43128657-G-A
• gnomAD v4: 10-43128657-G-A
• MyVariant Identifiers: chr10:g.43624105G>A (hg19) ; chr10:g.43128657G>A (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43128657G>A , CM000672.2:g.43128657G>A	GRCh38
NC_000010.10:g.43624105G>A , CM000672.1:g.43624105G>A	GRCh37
NC_000010.9:g.42944111G>A	NCBI36
NG_007489.1:g.56589G>A , LRG_518:g.56589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*1903G>A	ENSP00000480088.2:n.*1903G>A
ENST00000683007.1:n.4696G>A
ENST00000355710.8:c.*388G>A MANE Select	ENSP00000347942.3:n.*388G>A
ENST00000355710.7:c.*388G>A	ENSP00000347942.3:n.*388G>A
ENST00000615310.4:c.*1082G>A	ENSP00000480088.1:n.*1082G>A
NM_020975.4:c.*388G>A , LRG_518t1:c.*388G>A	NP_066124.1:n.*388G>A
XM_011540027.1:c.*16+372G>A	XP_011538329.1:n.*16+372G>A
NM_020975.5:c.*388G>A	NP_066124.1:n.*388G>A
NM_020975.6:c.*388G>A MANE Select	NP_066124.1:n.*388G>A