Canonical Allele Identifier: CA658832934

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[43118420G>A;43119548G>A] , CM000672.2:g.[43118420G>A;43119548G>A]	GRCh38
NC_000010.10:g.[43613868G>A;43614996G>A] , CM000672.1:g.[43613868G>A;43614996G>A]	GRCh37
NC_000010.9:g.[42933874G>A;42935002G>A]	NCBI36
NG_007489.1:g.[46352G>A;47480G>A] , LRG_518:g.[46352G>A;47480G>A]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.[1936G>A;2014G>A]	ENSP00000480088.2:p.[Val646Ile;Val672Met]
ENST00000683007.1:n.[1906G>A;1984G>A]
ENST00000683872.1:n.[1897G>A;1975G>A]
ENST00000340058.6:c.[2332G>A;2410G>A]	ENSP00000344798.4:p.[Val778Ile;Val804Met]
ENST00000355710.8:c.[2332G>A;2410G>A] MANE Select	ENSP00000347942.3:p.[Val778Ile;Val804Met]
ENST00000671844.1:c.[*926G>A;*1004G>A]	ENSP00000500541.1:n.[*926G>A;*1004G>A]
ENST00000672389.1:c.[*926G>A;*1004G>A]	ENSP00000500252.1:n.[*926G>A;*1004G>A]
ENST00000340058.5:c.[2332G>A;2410G>A]	ENSP00000344798.4:p.[Val778Ile;Val804Met]
ENST00000355710.7:c.[2332G>A;2410G>A]	ENSP00000347942.3:p.[Val778Ile;Val804Met]
ENST00000615310.4:c.[1290-1282G>A;1290-154G>A]	ENSP00000480088.1:n.[1290-1282G>A;1290-154G>A]
NM_020630.4:c.[2332G>A;2410G>A] , LRG_518t2:c.[2332G>A;2410G>A]	NP_065681.1:p.[Val778Ile;Val804Met]
NM_020975.4:c.[2332G>A;2410G>A] , LRG_518t1:c.[2332G>A;2410G>A]	NP_066124.1:p.[Val778Ile;Val804Met]
XM_011540027.1:c.[2332G>A;2410G>A]	XP_011538329.1:p.[Val778Ile;Val804Met]
NM_001355216.1:c.[1570G>A;1648G>A]	NP_001342145.1:p.[Val524Ile;Val550Met]
NM_020630.5:c.[2332G>A;2410G>A]	NP_065681.1:p.[Val778Ile;Val804Met]
NM_020975.5:c.[2332G>A;2410G>A]	NP_066124.1:p.[Val778Ile;Val804Met]
NM_020975.6:c.[2332G>A;2410G>A] MANE Select	NP_066124.1:p.[Val778Ile;Val804Met]
NM_020630.6:c.[2332G>A;2410G>A]	NP_065681.1:p.[Val778Ile;Val804Met]