Canonical Allele Identifier: CA645541265

Gene: RET

Linked Data

• COSMIC: COSM6191576

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120185_43120186delinsGG , CM000672.2:g.43120185_43120186delinsGG	GRCh38
NC_000010.10:g.43615633_43615634delinsGG , CM000672.1:g.43615633_43615634delinsGG	GRCh37
NC_000010.9:g.42935639_42935640delinsGG	NCBI36
NG_007489.1:g.48117_48118delinsGG , LRG_518:g.48117_48118delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2316_2317delinsGG	ENSP00000480088.2:p.Tyr773Asp
ENST00000683007.1:n.2286_2287delinsGG
ENST00000683872.1:n.2277_2278delinsGG
ENST00000340058.6:c.2712_2713delinsGG	ENSP00000344798.4:p.Tyr905Asp
ENST00000355710.8:c.2712_2713delinsGG MANE Select	ENSP00000347942.3:p.Tyr905Asp
ENST00000671844.1:c.*1306_*1307delinsGG	ENSP00000500541.1:n.*1306_*1307delinsGG
ENST00000672389.1:c.*1306_*1307delinsGG	ENSP00000500252.1:n.*1306_*1307delinsGG
ENST00000340058.5:c.2712_2713delinsGG	ENSP00000344798.4:p.Tyr905Asp
ENST00000355710.7:c.2712_2713delinsGG	ENSP00000347942.3:p.Tyr905Asp
ENST00000615310.4:c.*61_*62delinsGG	ENSP00000480088.1:n.*61_*62delinsGG
NM_020630.4:c.2712_2713delinsGG , LRG_518t2:c.2712_2713delinsGG	NP_065681.1:p.Tyr905Asp
NM_020975.4:c.2712_2713delinsGG , LRG_518t1:c.2712_2713delinsGG	NP_066124.1:p.Tyr905Asp
XM_011540027.1:c.2712_2713delinsGG	XP_011538329.1:p.Tyr905Asp
NM_001355216.1:c.1950_1951delinsGG	NP_001342145.1:p.Tyr651Asp
NM_020630.5:c.2712_2713delinsGG	NP_065681.1:p.Tyr905Asp
NM_020975.5:c.2712_2713delinsGG	NP_066124.1:p.Tyr905Asp
NM_020975.6:c.2712_2713delinsGG MANE Select	NP_066124.1:p.Tyr905Asp
NM_020630.6:c.2712_2713delinsGG	NP_065681.1:p.Tyr905Asp