Canonical Allele Identifier: CA2831039280

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118393_43118395delinsTTT , CM000672.2:g.43118393_43118395delinsTTT	GRCh38
NC_000010.10:g.43613841_43613843delinsTTT , CM000672.1:g.43613841_43613843delinsTTT	GRCh37
NC_000010.9:g.42933847_42933849delinsTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1909_1911delinsTTT	ENSP00000480088.2:p.Leu637Phe
ENST00000683007.1:n.1879_1881delinsTTT
ENST00000683872.1:n.1870_1872delinsTTT
ENST00000340058.6:c.2305_2307delinsTTT	ENSP00000344798.4:p.Leu769Phe
ENST00000355710.8:c.2305_2307delinsTTT MANE Select	ENSP00000347942.3:p.Leu769Phe
ENST00000671844.1:c.*899_*901delinsTTT	ENSP00000500541.1:n.*899_*901delinsTTT
ENST00000672389.1:c.*899_*901delinsTTT	ENSP00000500252.1:n.*899_*901delinsTTT
ENST00000340058.5:c.2305_2307delinsTTT	ENSP00000344798.4:p.Leu769Phe
ENST00000355710.7:c.2305_2307delinsTTT	ENSP00000347942.3:p.Leu769Phe
ENST00000615310.4:c.1290-1309_1290-1307delinsTTT	ENSP00000480088.1:n.1290-1309_1290-1307delinsTTT
XM_011540027.1:c.2305_2307delinsTTT	XP_011538329.1:p.Leu769Phe
NM_001355216.1:c.1543_1545delinsTTT	NP_001342145.1:p.Leu515Phe
NM_020630.5:c.2305_2307delinsTTT	NP_065681.1:p.Leu769Phe
NM_020975.5:c.2305_2307delinsTTT	NP_066124.1:p.Leu769Phe
NM_020975.6:c.2305_2307delinsTTT MANE Select	NP_066124.1:p.Leu769Phe
NM_020630.6:c.2305_2307delinsTTT	NP_065681.1:p.Leu769Phe