Canonical Allele Identifier: CA1905836562
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100067_43100068delinsAT , CM000672.2:g.43100067_43100068delinsAT GRCh38
NC_000010.10:g.43595515_43595516delinsAT , CM000672.1:g.43595515_43595516delinsAT GRCh37
NC_000010.9:g.42915521_42915522delinsAT NCBI36
NG_007489.1:g.27999_28000delinsAT , LRG_518:g.27999_28000delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.74-392_74-391delinsAT ENSP00000480088.2:n.74-392_74-391delinsAT
ENST00000340058.6:c.74-392_74-391delinsAT ENSP00000344798.4:n.74-392_74-391delinsAT
ENST00000355710.8:c.74-392_74-391delinsAT MANE Select ENSP00000347942.3:n.74-392_74-391delinsAT
ENST00000671844.1:c.74-392_74-391delinsAT ENSP00000500541.1:n.74-392_74-391delinsAT
ENST00000672389.1:c.74-11140_74-11139delinsAT ENSP00000500252.1:n.74-11140_74-11139delinsAT
ENST00000340058.5:c.74-392_74-391delinsAT ENSP00000344798.4:n.74-392_74-391delinsAT
ENST00000355710.7:c.74-392_74-391delinsAT ENSP00000347942.3:n.74-392_74-391delinsAT
ENST00000498820.5:c.74-12032_74-12031delinsAT ENSP00000419080.1:n.74-12032_74-12031delinsAT
ENST00000615310.4:c.74-392_74-391delinsAT ENSP00000480088.1:n.74-392_74-391delinsAT
NM_020630.4:c.74-392_74-391delinsAT , LRG_518t2:c.74-392_74-391delinsAT NP_065681.1:n.74-392_74-391delinsAT
NM_020975.4:c.74-392_74-391delinsAT , LRG_518t1:c.74-392_74-391delinsAT NP_066124.1:n.74-392_74-391delinsAT
XM_011540027.1:c.74-392_74-391delinsAT XP_011538329.1:n.74-392_74-391delinsAT
NM_020630.5:c.74-392_74-391delinsAT NP_065681.1:n.74-392_74-391delinsAT
NM_020975.5:c.74-392_74-391delinsAT NP_066124.1:n.74-392_74-391delinsAT
NM_020975.6:c.74-392_74-391delinsAT MANE Select NP_066124.1:n.74-392_74-391delinsAT
NM_020630.6:c.74-392_74-391delinsAT NP_065681.1:n.74-392_74-391delinsAT