Canonical Allele Identifier: CA915945897
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43111238_43111239delinsAG , CM000672.2:g.43111238_43111239delinsAG GRCh38
NC_000010.10:g.43606686_43606687delinsAG , CM000672.1:g.43606686_43606687delinsAG GRCh37
NC_000010.9:g.42926692_42926693delinsAG NCBI36
NG_007489.1:g.39170_39171delinsAG , LRG_518:g.39170_39171delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.899_900delinsAG ENSP00000480088.2:p.Ala300Glu
ENST00000683007.1:n.869_870delinsAG
ENST00000683872.1:n.56_57delinsAG
ENST00000340058.6:c.1295_1296delinsAG ENSP00000344798.4:p.Ala432Glu
ENST00000355710.8:c.1295_1296delinsAG MANE Select ENSP00000347942.3:p.Ala432Glu
ENST00000671844.1:c.657_658delinsAG ENSP00000500541.1:p.Ile220Val
ENST00000672389.1:c.105_106delinsAG ENSP00000500252.1:p.Ile36Val
ENST00000340058.5:c.1295_1296delinsAG ENSP00000344798.4:p.Ala432Glu
ENST00000355710.7:c.1295_1296delinsAG ENSP00000347942.3:p.Ala432Glu
ENST00000498820.5:c.74-861_74-860delinsAG ENSP00000419080.1:n.74-861_74-860delinsAG
ENST00000615310.4:c.1289+6_1289+7delinsAG ENSP00000480088.1:n.1289+6_1289+7delinsAG
NM_020630.4:c.1295_1296delinsAG , LRG_518t2:c.1295_1296delinsAG NP_065681.1:p.Ala432Glu
NM_020975.4:c.1295_1296delinsAG , LRG_518t1:c.1295_1296delinsAG NP_066124.1:p.Ala432Glu
XM_011540027.1:c.1295_1296delinsAG XP_011538329.1:p.Ala432Glu
NM_001355216.1:c.533_534delinsAG NP_001342145.1:p.Ala178Glu
NM_020630.5:c.1295_1296delinsAG NP_065681.1:p.Ala432Glu
NM_020975.5:c.1295_1296delinsAG NP_066124.1:p.Ala432Glu
NM_020975.6:c.1295_1296delinsAG MANE Select NP_066124.1:p.Ala432Glu
NM_020630.6:c.1295_1296delinsAG NP_065681.1:p.Ala432Glu