Canonical Allele Identifier: CA658832936

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[43118460A>T;43121968T>C] , CM000672.2:g.[43118460A>T;43121968T>C]	GRCh38
NC_000010.10:g.[43613908A>T;43617416T>C] , CM000672.1:g.[43613908A>T;43617416T>C]	GRCh37
NC_000010.9:g.[42933914A>T;42937422T>C]	NCBI36
NG_007489.1:g.[46392A>T;49900T>C] , LRG_518:g.[46392A>T;49900T>C]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.[1976A>T;2357T>C]	ENSP00000480088.2:p.[Tyr659Phe;Met786Thr]
ENST00000683007.1:n.[1946A>T;2327T>C]
ENST00000340058.6:c.[2372A>T;2753T>C]	ENSP00000344798.4:p.[Tyr791Phe;Met918Thr]
ENST00000355710.8:c.[2372A>T;2753T>C] MANE Select	ENSP00000347942.3:p.[Tyr791Phe;Met918Thr]
ENST00000671844.1:c.[*966A>T;*1347T>C]	ENSP00000500541.1:n.[*966A>T;*1347T>C]
ENST00000672389.1:c.[*966A>T;*1347T>C]	ENSP00000500252.1:n.[*966A>T;*1347T>C]
ENST00000340058.5:c.[2372A>T;2753T>C]	ENSP00000344798.4:p.[Tyr791Phe;Met918Thr]
ENST00000355710.7:c.[2372A>T;2753T>C]	ENSP00000347942.3:p.[Tyr791Phe;Met918Thr]
ENST00000615310.4:c.[1290-1242A>T;*102T>C]	ENSP00000480088.1:n.[1290-1242A>T;*102T>C]
NM_020630.4:c.[2372A>T;2753T>C] , LRG_518t2:c.[2372A>T;2753T>C]	NP_065681.1:p.[Tyr791Phe;Met918Thr]
NM_020975.4:c.[2372A>T;2753T>C] , LRG_518t1:c.[2372A>T;2753T>C]	NP_066124.1:p.[Tyr791Phe;Met918Thr]
XM_011540027.1:c.[2372A>T;2753T>C]	XP_011538329.1:p.[Tyr791Phe;Met918Thr]
NM_001355216.1:c.[1610A>T;1991T>C]	NP_001342145.1:p.[Tyr537Phe;Met664Thr]
NM_020630.5:c.[2372A>T;2753T>C]	NP_065681.1:p.[Tyr791Phe;Met918Thr]
NM_020975.5:c.[2372A>T;2753T>C]	NP_066124.1:p.[Tyr791Phe;Met918Thr]
NM_020975.6:c.[2372A>T;2753T>C] MANE Select	NP_066124.1:p.[Tyr791Phe;Met918Thr]
NM_020630.6:c.[2372A>T;2753T>C]	NP_065681.1:p.[Tyr791Phe;Met918Thr]