Canonical Allele Identifier: CA206266780

Gene: RET

Linked Data - Expert Curation

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120119_43120121delinsTTT , CM000672.2:g.43120119_43120121delinsTTT	GRCh38
NC_000010.10:g.43615567_43615569delinsTTT , CM000672.1:g.43615567_43615569delinsTTT	GRCh37
NC_000010.9:g.42935573_42935575delinsTTT	NCBI36
NG_007489.1:g.48051_48053delinsTTT , LRG_518:g.48051_48053delinsTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2250_2252delinsTTT	ENSP00000480088.2:p.Ala751Phe
ENST00000683007.1:n.2220_2222delinsTTT
ENST00000683872.1:n.2211_2213delinsTTT
ENST00000340058.6:c.2646_2648delinsTTT	ENSP00000344798.4:p.Ala883Phe
ENST00000355710.8:c.2646_2648delinsTTT MANE Select	ENSP00000347942.3:p.Ala883Phe
ENST00000671844.1:c.*1240_*1242delinsTTT	ENSP00000500541.1:n.*1240_*1242delinsTTT
ENST00000672389.1:c.*1240_*1242delinsTTT	ENSP00000500252.1:n.*1240_*1242delinsTTT
ENST00000340058.5:c.2646_2648delinsTTT	ENSP00000344798.4:p.Ala883Phe
ENST00000355710.7:c.2646_2648delinsTTT	ENSP00000347942.3:p.Ala883Phe
ENST00000615310.4:c.1372_1374delinsTTT	ENSP00000480088.1:p.Ser458Phe
NM_020630.4:c.2646_2648delinsTTT , LRG_518t2:c.2646_2648delinsTTT	NP_065681.1:p.Ala883Phe
NM_020975.4:c.2646_2648delinsTTT , LRG_518t1:c.2646_2648delinsTTT	NP_066124.1:p.Ala883Phe
XM_011540027.1:c.2646_2648delinsTTT	XP_011538329.1:p.Ala883Phe
NM_001355216.1:c.1884_1886delinsTTT	NP_001342145.1:p.Ala629Phe
NM_020630.5:c.2646_2648delinsTTT	NP_065681.1:p.Ala883Phe
NM_020975.5:c.2646_2648delinsTTT	NP_066124.1:p.Ala883Phe
NM_020975.6:c.2646_2648delinsTTT MANE Select	NP_066124.1:p.Ala883Phe
NM_020630.6:c.2646_2648delinsTTT	NP_065681.1:p.Ala883Phe