Canonical Allele Identifier: CA2547121100
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43130305-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130305G>T , CM000672.2:g.43130305G>T GRCh38
NC_000010.10:g.43625753G>T , CM000672.1:g.43625753G>T GRCh37
NC_000010.9:g.42945759G>T NCBI36
NG_007489.1:g.58237G>T , LRG_518:g.58237G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2036G>T MANE Select ENSP00000347942.3:n.*2036G>T
ENST00000355710.7:c.*2036G>T ENSP00000347942.3:n.*2036G>T
ENST00000615310.4:c.*2730G>T ENSP00000480088.1:n.*2730G>T
NM_020975.4:c.*2036G>T , LRG_518t1:c.*2036G>T NP_066124.1:n.*2036G>T
XM_011540027.1:c.*804G>T XP_011538329.1:n.*804G>T
NM_020975.5:c.*2036G>T NP_066124.1:n.*2036G>T
NM_020975.6:c.*2036G>T MANE Select NP_066124.1:n.*2036G>T
Search 100 bp 5'
Search 100 bp 3'