Canonical Allele Identifier: CA2608897191
Gene: RET HGNC NCBI

Linked Data

gnomAD v4: 10-43130296-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43130296T>C , CM000672.2:g.43130296T>C GRCh38
NC_000010.10:g.43625744T>C , CM000672.1:g.43625744T>C GRCh37
NC_000010.9:g.42945750T>C NCBI36
NG_007489.1:g.58228T>C , LRG_518:g.58228T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000355710.8:c.*2027T>C MANE Select ENSP00000347942.3:n.*2027T>C
ENST00000355710.7:c.*2027T>C ENSP00000347942.3:n.*2027T>C
ENST00000615310.4:c.*2721T>C ENSP00000480088.1:n.*2721T>C
NM_020975.4:c.*2027T>C , LRG_518t1:c.*2027T>C NP_066124.1:n.*2027T>C
XM_011540027.1:c.*795T>C XP_011538329.1:n.*795T>C
NM_020975.5:c.*2027T>C NP_066124.1:n.*2027T>C
NM_020975.6:c.*2027T>C MANE Select NP_066124.1:n.*2027T>C
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