Canonical Allele Identifier: CA2608875779
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119982_43119983dup , CM000672.2:g.43119982_43119983dup GRCh38
NC_000010.10:g.43615430_43615431dup , CM000672.1:g.43615430_43615431dup GRCh37
NC_000010.9:g.42935436_42935437dup NCBI36
NG_007489.1:g.47914_47915dup , LRG_518:g.47914_47915dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2212-99_2212-98dup ENSP00000480088.2:n.2212-99_2212-98dup
ENST00000683007.1:n.2182-99_2182-98dup
ENST00000683872.1:n.2173-99_2173-98dup
ENST00000340058.6:c.2608-99_2608-98dup ENSP00000344798.4:n.2608-99_2608-98dup
ENST00000355710.8:c.2608-99_2608-98dup MANE Select ENSP00000347942.3:n.2608-99_2608-98dup
ENST00000671844.1:c.*1202-99_*1202-98dup ENSP00000500541.1:n.*1202-99_*1202-98dup
ENST00000672389.1:c.*1202-99_*1202-98dup ENSP00000500252.1:n.*1202-99_*1202-98dup
ENST00000340058.5:c.2608-99_2608-98dup ENSP00000344798.4:n.2608-99_2608-98dup
ENST00000355710.7:c.2608-99_2608-98dup ENSP00000347942.3:n.2608-99_2608-98dup
ENST00000615310.4:c.1334-99_1334-98dup ENSP00000480088.1:n.1334-99_1334-98dup
NM_020630.4:c.2608-99_2608-98dup , LRG_518t2:c.2608-99_2608-98dup NP_065681.1:n.2608-99_2608-98dup
NM_020975.4:c.2608-99_2608-98dup , LRG_518t1:c.2608-99_2608-98dup NP_066124.1:n.2608-99_2608-98dup
XM_011540027.1:c.2608-99_2608-98dup XP_011538329.1:n.2608-99_2608-98dup
NM_001355216.1:c.1846-99_1846-98dup NP_001342145.1:n.1846-99_1846-98dup
NM_020630.5:c.2608-99_2608-98dup NP_065681.1:n.2608-99_2608-98dup
NM_020975.5:c.2608-99_2608-98dup NP_066124.1:n.2608-99_2608-98dup
NM_020975.6:c.2608-99_2608-98dup MANE Select NP_066124.1:n.2608-99_2608-98dup
NM_020630.6:c.2608-99_2608-98dup NP_065681.1:n.2608-99_2608-98dup