Canonical Allele Identifier: CA356501

Gene: RET

Linked Data

• PubMed: PMID:3078962 ; PMID:7907913 ; PMID:8099202

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[43114496G>C;43114497C>G;43114500T>C] , CM000672.2:g.[43114496G>C;43114497C>G;43114500T>C]	GRCh38
NC_000010.10:g.[43609944G>C;43609945C>G;43609948T>C] , CM000672.1:g.[43609944G>C;43609945C>G;43609948T>C]	GRCh37
NC_000010.9:g.[42929950G>C;42929951C>G;42929954T>C]	NCBI36
NG_007489.1:g.[42428G>C;42429C>G;42432T>C] , LRG_518:g.[42428G>C;42429C>G;42432T>C]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.[1500G>C;1501C>G;1504T>C]	ENSP00000480088.2:p.[Glu500_Leu501delinsAspVal;Cys502Arg]
ENST00000683007.1:n.[1470G>C;1471C>G;1474T>C]
ENST00000683872.1:n.[1461G>C;1462C>G;1465T>C]
ENST00000340058.6:c.[1896G>C;1897C>G;1900T>C]	ENSP00000344798.4:p.[Glu632Asp;Leu633Val;Cys634Arg]
ENST00000355710.8:c.[1896G>C;1897C>G;1900T>C] MANE Select	ENSP00000347942.3:p.[Glu632Asp;Leu633Val;Cys634Arg]
ENST00000671844.1:c.[*490G>C;*491C>G;*494T>C]	ENSP00000500541.1:n.[*490G>C;*491C>G;*494T>C]
ENST00000672389.1:c.[*490G>C;*491C>G;*494T>C]	ENSP00000500252.1:n.[*490G>C;*491C>G;*494T>C]
ENST00000340058.5:c.[1896G>C;1897C>G;1900T>C]	ENSP00000344798.4:p.[Glu632_Leu633delinsAspVal;Cys634Arg]
ENST00000355710.7:c.[1896G>C;1897C>G;1900T>C]	ENSP00000347942.3:p.[Glu632Asp;Leu633Val;Cys634Arg]
ENST00000498820.5:c.[447G>C;448C>G;451T>C]	ENSP00000419080.1:p.[Glu149_Leu150delinsAspVal;Cys151Arg]
ENST00000615310.4:c.[1289+3264G>C;1289+3265C>G;1289+3268T>C]	ENSP00000480088.1:n.[1289+3264G>C;1289+3265C>G;1289+3268T>C]
NM_020630.4:c.[1896G>C;1897C>G;1900T>C] , LRG_518t2:c.[1896G>C;1897C>G;1900T>C]	NP_065681.1:p.[Glu632Asp;Leu633Val;Cys634Arg]
NM_020975.4:c.[1896G>C;1897C>G;1900T>C] , LRG_518t1:c.[1896G>C;1897C>G;1900T>C]	NP_066124.1:p.[Glu632Asp;Leu633Val;Cys634Arg]
XM_011540027.1:c.[1896G>C;1897C>G;1900T>C]	XP_011538329.1:p.[Glu632Asp;Leu633Val;Cys634Arg]
NM_001355216.1:c.[1134G>C;1135C>G;1138T>C]	NP_001342145.1:p.[Glu378_Leu379delinsAspVal;Cys380Arg]
NM_020630.5:c.[1896G>C;1897C>G;1900T>C]	NP_065681.1:p.[Glu632Asp;Leu633Val;Cys634Arg]
NM_020975.5:c.[1896G>C;1897C>G;1900T>C]	NP_066124.1:p.[Glu632Asp;Leu633Val;Cys634Arg]
NM_020975.6:c.[1896G>C;1897C>G;1900T>C] MANE Select	NP_066124.1:p.[Glu632Asp;Leu633Val;Cys634Arg]
NM_020630.6:c.[1896G>C;1897C>G;1900T>C]	NP_065681.1:p.[Glu632Asp;Leu633Val;Cys634Arg]