Canonical Allele Identifier: CA658832939

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[43119548G>A;43119669G>T] , CM000672.2:g.[43119548G>A;43119669G>T]	GRCh38
NC_000010.10:g.[43614996G>A;43615117G>T] , CM000672.1:g.[43614996G>A;43615117G>T]	GRCh37
NC_000010.9:g.[42935002G>A;42935123G>T]	NCBI36
NG_007489.1:g.[47480G>A;47601G>T] , LRG_518:g.[47480G>A;47601G>T]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.[2014G>A;2135G>T]	ENSP00000480088.2:p.[Val672Met;Arg712Leu]
ENST00000683007.1:n.[1984G>A;2105G>T]
ENST00000683872.1:n.[1975G>A;2096G>T]
ENST00000340058.6:c.[2410G>A;2531G>T]	ENSP00000344798.4:p.[Val804Met;Arg844Leu]
ENST00000355710.8:c.[2410G>A;2531G>T] MANE Select	ENSP00000347942.3:p.[Val804Met;Arg844Leu]
ENST00000671844.1:c.[*1004G>A;*1125G>T]	ENSP00000500541.1:n.[*1004G>A;*1125G>T]
ENST00000672389.1:c.[*1004G>A;*1125G>T]	ENSP00000500252.1:n.[*1004G>A;*1125G>T]
ENST00000340058.5:c.[2410G>A;2531G>T]	ENSP00000344798.4:p.[Val804Met;Arg844Leu]
ENST00000355710.7:c.[2410G>A;2531G>T]	ENSP00000347942.3:p.[Val804Met;Arg844Leu]
ENST00000615310.4:c.[1290-154G>A;1290-33G>T]	ENSP00000480088.1:n.[1290-154G>A;1290-33G>T]
NM_020630.4:c.[2410G>A;2531G>T] , LRG_518t2:c.[2410G>A;2531G>T]	NP_065681.1:p.[Val804Met;Arg844Leu]
NM_020975.4:c.[2410G>A;2531G>T] , LRG_518t1:c.[2410G>A;2531G>T]	NP_066124.1:p.[Val804Met;Arg844Leu]
XM_011540027.1:c.[2410G>A;2531G>T]	XP_011538329.1:p.[Val804Met;Arg844Leu]
NM_001355216.1:c.[1648G>A;1769G>T]	NP_001342145.1:p.[Val550Met;Arg590Leu]
NM_020630.5:c.[2410G>A;2531G>T]	NP_065681.1:p.[Val804Met;Arg844Leu]
NM_020975.5:c.[2410G>A;2531G>T]	NP_066124.1:p.[Val804Met;Arg844Leu]
NM_020975.6:c.[2410G>A;2531G>T] MANE Select	NP_066124.1:p.[Val804Met;Arg844Leu]
NM_020630.6:c.[2410G>A;2531G>T]	NP_065681.1:p.[Val804Met;Arg844Leu]