Canonical Allele Identifier: CA10628576

Gene: RET

Linked Data

• ClinVar Variation Id: 299924
• ClinVar RCV Id: RCV000263902 ; RCV000319027 ; RCV000373474 ; RCV000367893
• dbSNP Id: rs886047006
• gnomAD v3: 10-43129378-T-C
• gnomAD v4: 10-43129378-T-C
• MyVariant Identifiers: chr10:g.43624826T>C (hg19) ; chr10:g.43129378T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43129378T>C , CM000672.2:g.43129378T>C	GRCh38
NC_000010.10:g.43624826T>C , CM000672.1:g.43624826T>C	GRCh37
NC_000010.9:g.42944832T>C	NCBI36
NG_007489.1:g.57310T>C , LRG_518:g.57310T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*2624T>C	ENSP00000480088.2:n.*2624T>C
ENST00000683007.1:n.5417T>C
ENST00000355710.8:c.*1109T>C MANE Select	ENSP00000347942.3:n.*1109T>C
ENST00000355710.7:c.*1109T>C	ENSP00000347942.3:n.*1109T>C
ENST00000615310.4:c.*1803T>C	ENSP00000480088.1:n.*1803T>C
NM_020975.4:c.*1109T>C , LRG_518t1:c.*1109T>C	NP_066124.1:n.*1109T>C
XM_011540027.1:c.*17-140T>C	XP_011538329.1:n.*17-140T>C
NM_020975.5:c.*1109T>C	NP_066124.1:n.*1109T>C
NM_020975.6:c.*1109T>C MANE Select	NP_066124.1:n.*1109T>C