Canonical Allele Identifier: CA10631689

Gene: RET

Linked Data

• ClinVar Variation Id: 299939
• ClinVar RCV Id: RCV000276517 ; RCV000331623 ; RCV000356657 ; RCV000370937
• dbSNP Id: rs117119161
• gnomAD v2: 10-43625361-G-C
• gnomAD v3: 10-43129913-G-C
• gnomAD v4: 10-43129913-G-C
• MyVariant Identifiers: chr10:g.43625361G>C (hg19) ; chr10:g.43129913G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43129913G>C , CM000672.2:g.43129913G>C	GRCh38
NC_000010.10:g.43625361G>C , CM000672.1:g.43625361G>C	GRCh37
NC_000010.9:g.42945367G>C	NCBI36
NG_007489.1:g.57845G>C , LRG_518:g.57845G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3159G>C	ENSP00000480088.2:n.*3159G>C
ENST00000683007.1:n.5952G>C
ENST00000355710.8:c.*1644G>C MANE Select	ENSP00000347942.3:n.*1644G>C
ENST00000355710.7:c.*1644G>C	ENSP00000347942.3:n.*1644G>C
ENST00000615310.4:c.*2338G>C	ENSP00000480088.1:n.*2338G>C
NM_020975.4:c.*1644G>C , LRG_518t1:c.*1644G>C	NP_066124.1:n.*1644G>C
XM_011540027.1:c.*412G>C	XP_011538329.1:n.*412G>C
NM_020975.5:c.*1644G>C	NP_066124.1:n.*1644G>C
NM_020975.6:c.*1644G>C MANE Select	NP_066124.1:n.*1644G>C