Canonical Allele Identifier: CA2841991398
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119589_43119590insA , CM000672.2:g.43119589_43119590insA GRCh38
NC_000010.10:g.43615037_43615038insA , CM000672.1:g.43615037_43615038insA GRCh37
NC_000010.9:g.42935043_42935044insA NCBI36
NG_007489.1:g.47521_47522insA , LRG_518:g.47521_47522insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2055_2056insA ENSP00000480088.2:p.Glu686ArgfsTer26
ENST00000683007.1:n.2025_2026insA
ENST00000683872.1:n.2016_2017insA
ENST00000340058.6:c.2451_2452insA ENSP00000344798.4:p.Glu818ArgfsTer26
ENST00000355710.8:c.2451_2452insA MANE Select ENSP00000347942.3:p.Glu818ArgfsTer26
ENST00000671844.1:c.*1045_*1046insA ENSP00000500541.1:n.*1045_*1046insA
ENST00000672389.1:c.*1045_*1046insA ENSP00000500252.1:n.*1045_*1046insA
ENST00000340058.5:c.2451_2452insA ENSP00000344798.4:p.Glu818ArgfsTer26
ENST00000355710.7:c.2451_2452insA ENSP00000347942.3:p.Glu818ArgfsTer26
ENST00000615310.4:c.1290-113_1290-112insA ENSP00000480088.1:n.1290-113_1290-112insA
NM_020630.4:c.2451_2452insA , LRG_518t2:c.2451_2452insA NP_065681.1:p.Glu818ArgfsTer26
NM_020975.4:c.2451_2452insA , LRG_518t1:c.2451_2452insA NP_066124.1:p.Glu818ArgfsTer26
XM_011540027.1:c.2451_2452insA XP_011538329.1:p.Glu818ArgfsTer26
NM_001355216.1:c.1689_1690insA NP_001342145.1:p.Glu564ArgfsTer26
NM_020630.5:c.2451_2452insA NP_065681.1:p.Glu818ArgfsTer26
NM_020975.5:c.2451_2452insA NP_066124.1:p.Glu818ArgfsTer26
NM_020975.6:c.2451_2452insA MANE Select NP_066124.1:p.Glu818ArgfsTer26
NM_020630.6:c.2451_2452insA NP_065681.1:p.Glu818ArgfsTer26