Canonical Allele Identifier: CA2608872511
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43114400_43114402del , CM000672.2:g.43114400_43114402del GRCh38
NC_000010.10:g.43609848_43609850del , CM000672.1:g.43609848_43609850del GRCh37
NC_000010.9:g.42929854_42929856del NCBI36
NG_007489.1:g.42332_42334del , LRG_518:g.42332_42334del

Transcript Alleles

HGVS Amino-acid change
ENST00000615310.5:c.1484-80_1484-78del ENSP00000480088.2:n.1484-80_1484-78del
ENST00000683007.1:n.1454-80_1454-78del
ENST00000683872.1:n.1365_1367del
ENST00000340058.6:c.1880-80_1880-78del ENSP00000344798.4:n.1880-80_1880-78del
ENST00000355710.8:c.1880-80_1880-78del MANE Select ENSP00000347942.3:n.1880-80_1880-78del
ENST00000671844.1:c.*474-80_*474-78del ENSP00000500541.1:n.*474-80_*474-78del
ENST00000672389.1:c.*474-80_*474-78del ENSP00000500252.1:n.*474-80_*474-78del
ENST00000340058.5:c.1880-80_1880-78del ENSP00000344798.4:n.1880-80_1880-78del
ENST00000355710.7:c.1880-80_1880-78del ENSP00000347942.3:n.1880-80_1880-78del
ENST00000498820.5:c.431-80_431-78del ENSP00000419080.1:n.431-80_431-78del
ENST00000615310.4:c.1289+3168_1289+3170del ENSP00000480088.1:n.1289+3168_1289+3170de...
NM_020630.4:c.1880-80_1880-78del , LRG_518t2:c.1880-80_1880-78del NP_065681.1:n.1880-80_1880-78del
NM_020975.4:c.1880-80_1880-78del , LRG_518t1:c.1880-80_1880-78del NP_066124.1:n.1880-80_1880-78del
XM_011540027.1:c.1880-80_1880-78del XP_011538329.1:n.1880-80_1880-78del
NM_001355216.1:c.1118-80_1118-78del NP_001342145.1:n.1118-80_1118-78del
NM_020630.5:c.1880-80_1880-78del NP_065681.1:n.1880-80_1880-78del
NM_020975.5:c.1880-80_1880-78del NP_066124.1:n.1880-80_1880-78del
NM_020975.6:c.1880-80_1880-78del MANE Select NP_066124.1:n.1880-80_1880-78del
NM_020630.6:c.1880-80_1880-78del NP_065681.1:n.1880-80_1880-78del