Canonical Allele Identifier: CA645541262

Gene: RET

Linked Data

• ClinVar Variation Id: 3072428
• ClinVar RCV Id: RCV004013450
• COSMIC: COSM5030969

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120184_43120185delinsTG , CM000672.2:g.43120184_43120185delinsTG	GRCh38
NC_000010.10:g.43615632_43615633delinsTG , CM000672.1:g.43615632_43615633delinsTG	GRCh37
NC_000010.9:g.42935638_42935639delinsTG	NCBI36
NG_007489.1:g.48116_48117delinsTG , LRG_518:g.48116_48117delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.2315_2316delinsTG	ENSP00000480088.2:p.Ser772Leu
ENST00000683007.1:n.2285_2286delinsTG
ENST00000683872.1:n.2276_2277delinsTG
ENST00000340058.6:c.2711_2712delinsTG	ENSP00000344798.4:p.Ser904Leu
ENST00000355710.8:c.2711_2712delinsTG MANE Select	ENSP00000347942.3:p.Ser904Leu
ENST00000671844.1:c.*1305_*1306delinsTG	ENSP00000500541.1:n.*1305_*1306delinsTG
ENST00000672389.1:c.*1305_*1306delinsTG	ENSP00000500252.1:n.*1305_*1306delinsTG
ENST00000340058.5:c.2711_2712delinsTG	ENSP00000344798.4:p.Ser904Leu
ENST00000355710.7:c.2711_2712delinsTG	ENSP00000347942.3:p.Ser904Leu
ENST00000615310.4:c.*60_*61delinsTG	ENSP00000480088.1:n.*60_*61delinsTG
NM_020630.4:c.2711_2712delinsTG , LRG_518t2:c.2711_2712delinsTG	NP_065681.1:p.Ser904Leu
NM_020975.4:c.2711_2712delinsTG , LRG_518t1:c.2711_2712delinsTG	NP_066124.1:p.Ser904Leu
XM_011540027.1:c.2711_2712delinsTG	XP_011538329.1:p.Ser904Leu
NM_001355216.1:c.1949_1950delinsTG	NP_001342145.1:p.Ser650Leu
NM_020630.5:c.2711_2712delinsTG	NP_065681.1:p.Ser904Leu
NM_020975.5:c.2711_2712delinsTG	NP_066124.1:p.Ser904Leu
NM_020975.6:c.2711_2712delinsTG MANE Select	NP_066124.1:p.Ser904Leu
NM_020630.6:c.2711_2712delinsTG	NP_065681.1:p.Ser904Leu