Canonical Allele Identifier: CA206268550
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 879260
ClinVar RCV Id: RCV001106587 RCV001106588 RCV001106589 RCV001106590
dbSNP Id: rs956882000
gnomAD v2: 10-43625617-C-A
gnomAD v3: 10-43130169-C-A
gnomAD v4: 10-43130169-C-A
MyVariant Identifiers: chr10:g.43625617C>A (hg19) chr10:g.43130169C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130169C>A , CM000672.2:g.43130169C>A GRCh38
NC_000010.10:g.43625617C>A , CM000672.1:g.43625617C>A GRCh37
NC_000010.9:g.42945623C>A NCBI36
NG_007489.1:g.58101C>A , LRG_518:g.58101C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3415C>A ENSP00000480088.2:n.*3415C>A
ENST00000683007.1:n.6208C>A
ENST00000355710.8:c.*1900C>A MANE Select ENSP00000347942.3:n.*1900C>A
ENST00000355710.7:c.*1900C>A ENSP00000347942.3:n.*1900C>A
ENST00000615310.4:c.*2594C>A ENSP00000480088.1:n.*2594C>A
NM_020975.4:c.*1900C>A , LRG_518t1:c.*1900C>A NP_066124.1:n.*1900C>A
XM_011540027.1:c.*668C>A XP_011538329.1:n.*668C>A
NM_020975.5:c.*1900C>A NP_066124.1:n.*1900C>A
NM_020975.6:c.*1900C>A MANE Select NP_066124.1:n.*1900C>A
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