Canonical Allele Identifier: CA2608897166
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43130167-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130167T>C , CM000672.2:g.43130167T>C GRCh38
NC_000010.10:g.43625615T>C , CM000672.1:g.43625615T>C GRCh37
NC_000010.9:g.42945621T>C NCBI36
NG_007489.1:g.58099T>C , LRG_518:g.58099T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.*3413T>C ENSP00000480088.2:n.*3413T>C
ENST00000683007.1:n.6206T>C
ENST00000355710.8:c.*1898T>C MANE Select ENSP00000347942.3:n.*1898T>C
ENST00000355710.7:c.*1898T>C ENSP00000347942.3:n.*1898T>C
ENST00000615310.4:c.*2592T>C ENSP00000480088.1:n.*2592T>C
NM_020975.4:c.*1898T>C , LRG_518t1:c.*1898T>C NP_066124.1:n.*1898T>C
XM_011540027.1:c.*666T>C XP_011538329.1:n.*666T>C
NM_020975.5:c.*1898T>C NP_066124.1:n.*1898T>C
NM_020975.6:c.*1898T>C MANE Select NP_066124.1:n.*1898T>C
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