Canonical Allele Identifier: CA645541261
Gene: RET HGNC NCBI

Linked Data

COSMIC: COSM374956

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119717_43119718delinsCA , CM000672.2:g.43119717_43119718delinsCA GRCh38
NC_000010.10:g.43615165_43615166delinsCA , CM000672.1:g.43615165_43615166delinsCA GRCh37
NC_000010.9:g.42935171_42935172delinsCA NCBI36
NG_007489.1:g.47649_47650delinsCA , LRG_518:g.47649_47650delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2183_2184delinsCA ENSP00000480088.2:p.Gln728Pro
ENST00000683007.1:n.2153_2154delinsCA
ENST00000683872.1:n.2144_2145delinsCA
ENST00000340058.6:c.2579_2580delinsCA ENSP00000344798.4:p.Gln860Pro
ENST00000355710.8:c.2579_2580delinsCA MANE Select ENSP00000347942.3:p.Gln860Pro
ENST00000671844.1:c.*1173_*1174delinsCA ENSP00000500541.1:n.*1173_*1174delinsCA
ENST00000672389.1:c.*1173_*1174delinsCA ENSP00000500252.1:n.*1173_*1174delinsCA
ENST00000340058.5:c.2579_2580delinsCA ENSP00000344798.4:p.Gln860Pro
ENST00000355710.7:c.2579_2580delinsCA ENSP00000347942.3:p.Gln860Pro
ENST00000615310.4:c.1305_1306delinsCA ENSP00000480088.1:p.Gly436Arg
NM_020630.4:c.2579_2580delinsCA , LRG_518t2:c.2579_2580delinsCA NP_065681.1:p.Gln860Pro
NM_020975.4:c.2579_2580delinsCA , LRG_518t1:c.2579_2580delinsCA NP_066124.1:p.Gln860Pro
XM_011540027.1:c.2579_2580delinsCA XP_011538329.1:p.Gln860Pro
NM_001355216.1:c.1817_1818delinsCA NP_001342145.1:p.Gln606Pro
NM_020630.5:c.2579_2580delinsCA NP_065681.1:p.Gln860Pro
NM_020975.5:c.2579_2580delinsCA NP_066124.1:p.Gln860Pro
NM_020975.6:c.2579_2580delinsCA MANE Select NP_066124.1:p.Gln860Pro
NM_020630.6:c.2579_2580delinsCA NP_065681.1:p.Gln860Pro