Canonical Allele Identifier: CA927692516
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs1837605999

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100187_43100188del , CM000672.2:g.43100187_43100188del GRCh38
NC_000010.10:g.43595635_43595636del , CM000672.1:g.43595635_43595636del GRCh37
NC_000010.9:g.42915641_42915642del NCBI36
NG_007489.1:g.28119_28120del , LRG_518:g.28119_28120del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.74-272_74-271del ENSP00000480088.2:n.74-272_74-271del
ENST00000340058.6:c.74-272_74-271del ENSP00000344798.4:n.74-272_74-271del
ENST00000355710.8:c.74-272_74-271del MANE Select ENSP00000347942.3:n.74-272_74-271del
ENST00000671844.1:c.74-272_74-271del ENSP00000500541.1:n.74-272_74-271del
ENST00000672389.1:c.74-11020_74-11019del ENSP00000500252.1:n.74-11020_74-11019del
ENST00000340058.5:c.74-272_74-271del ENSP00000344798.4:n.74-272_74-271del
ENST00000355710.7:c.74-272_74-271del ENSP00000347942.3:n.74-272_74-271del
ENST00000498820.5:c.74-11912_74-11911del ENSP00000419080.1:n.74-11912_74-11911del
ENST00000615310.4:c.74-272_74-271del ENSP00000480088.1:n.74-272_74-271del
NM_020630.4:c.74-272_74-271del , LRG_518t2:c.74-272_74-271del NP_065681.1:n.74-272_74-271del
NM_020975.4:c.74-272_74-271del , LRG_518t1:c.74-272_74-271del NP_066124.1:n.74-272_74-271del
XM_011540027.1:c.74-272_74-271del XP_011538329.1:n.74-272_74-271del
NM_020630.5:c.74-272_74-271del NP_065681.1:n.74-272_74-271del
NM_020975.5:c.74-272_74-271del NP_066124.1:n.74-272_74-271del
NM_020975.6:c.74-272_74-271del MANE Select NP_066124.1:n.74-272_74-271del
NM_020630.6:c.74-272_74-271del NP_065681.1:n.74-272_74-271del