Canonical Allele Identifier: CA2695211966
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100540_43100543del , CM000672.2:g.43100540_43100543del GRCh38
NC_000010.10:g.43595988_43595991del , CM000672.1:g.43595988_43595991del GRCh37
NC_000010.9:g.42915994_42915997del NCBI36
NG_007489.1:g.28472_28475del , LRG_518:g.28472_28475del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.155_158del ENSP00000480088.2:p.Tyr52SerfsTer?
ENST00000683278.1:c.57_60del
ENST00000684216.1:c.57_60del
ENST00000340058.6:c.155_158del ENSP00000344798.4:p.Tyr52SerfsTer?
ENST00000355710.8:c.155_158del MANE Select ENSP00000347942.3:p.Tyr52SerfsTer?
ENST00000638465.1:c.57_60del
ENST00000640619.1:c.57_60del
ENST00000671844.1:c.155_158del ENSP00000500541.1:p.Tyr52SerfsTer?
ENST00000672389.1:c.74-10667_74-10664del ENSP00000500252.1:n.74-10667_74-10664del
ENST00000340058.5:c.155_158del ENSP00000344798.4:p.Tyr52SerfsTer?
ENST00000355710.7:c.155_158del ENSP00000347942.3:p.Tyr52SerfsTer?
ENST00000498820.5:c.74-11559_74-11556del ENSP00000419080.1:n.74-11559_74-11556del
ENST00000615310.4:c.155_158del ENSP00000480088.1:p.Tyr52SerfsTer?
NM_020630.4:c.155_158del , LRG_518t2:c.155_158del NP_065681.1:p.Tyr52SerfsTer?
NM_020975.4:c.155_158del , LRG_518t1:c.155_158del NP_066124.1:p.Tyr52SerfsTer?
XM_011540027.1:c.155_158del XP_011538329.1:p.Tyr52SerfsTer?
NM_020630.5:c.155_158del NP_065681.1:p.Tyr52SerfsTer?
NM_020975.5:c.155_158del NP_066124.1:p.Tyr52SerfsTer?
NM_020975.6:c.155_158del MANE Select NP_066124.1:p.Tyr52SerfsTer?
NM_020630.6:c.155_158del NP_065681.1:p.Tyr52SerfsTer?