Canonical Allele Identifier: CA592898376
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1236953903
gnomAD v2: 10-43625715-G-A
gnomAD v3: 10-43130267-G-A
gnomAD v4: 10-43130267-G-A
MyVariant Identifiers: chr10:g.43625715G>A (hg19) chr10:g.43130267G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130267G>A , CM000672.2:g.43130267G>A GRCh38
NC_000010.10:g.43625715G>A , CM000672.1:g.43625715G>A GRCh37
NC_000010.9:g.42945721G>A NCBI36
NG_007489.1:g.58199G>A , LRG_518:g.58199G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3513G>A ENSP00000480088.2:n.*3513G>A
ENST00000683007.1:n.6306G>A
ENST00000355710.8:c.*1998G>A MANE Select ENSP00000347942.3:n.*1998G>A
ENST00000355710.7:c.*1998G>A ENSP00000347942.3:n.*1998G>A
ENST00000615310.4:c.*2692G>A ENSP00000480088.1:n.*2692G>A
NM_020975.4:c.*1998G>A , LRG_518t1:c.*1998G>A NP_066124.1:n.*1998G>A
XM_011540027.1:c.*766G>A XP_011538329.1:n.*766G>A
NM_020975.5:c.*1998G>A NP_066124.1:n.*1998G>A
NM_020975.6:c.*1998G>A MANE Select NP_066124.1:n.*1998G>A
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