Canonical Allele Identifier: CA2608897190
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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