Canonical Allele Identifier: CA665316823
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1366966529
MyVariant Identifiers: chr10:g.43625729T>A (hg19) chr10:g.43130281T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130281T>A , CM000672.2:g.43130281T>A GRCh38
NC_000010.10:g.43625729T>A , CM000672.1:g.43625729T>A GRCh37
NC_000010.9:g.42945735T>A NCBI36
NG_007489.1:g.58213T>A , LRG_518:g.58213T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2012T>A MANE Select ENSP00000347942.3:n.*2012T>A
ENST00000355710.7:c.*2012T>A ENSP00000347942.3:n.*2012T>A
ENST00000615310.4:c.*2706T>A ENSP00000480088.1:n.*2706T>A
NM_020975.4:c.*2012T>A , LRG_518t1:c.*2012T>A NP_066124.1:n.*2012T>A
XM_011540027.1:c.*780T>A XP_011538329.1:n.*780T>A
NM_020975.5:c.*2012T>A NP_066124.1:n.*2012T>A
NM_020975.6:c.*2012T>A MANE Select NP_066124.1:n.*2012T>A
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