Canonical Allele Identifier: CA356502

Gene: RET

Linked Data

• PubMed: PMID:11788682

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.[43119548G>A;43120184C>G] , CM000672.2:g.[43119548G>A;43120184C>G]	GRCh38
NC_000010.10:g.[43614996G>A;43615632C>G] , CM000672.1:g.[43614996G>A;43615632C>G]	GRCh37
NC_000010.9:g.[42935002G>A;42935638C>G]	NCBI36
NG_007489.1:g.[47480G>A;48116C>G] , LRG_518:g.[47480G>A;48116C>G]

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.[2014G>A;2315C>G]	ENSP00000480088.2:p.[Val672Met;Ser772Cys]
ENST00000683007.1:n.[1984G>A;2285C>G]
ENST00000683872.1:n.[1975G>A;2276C>G]
ENST00000340058.6:c.[2410G>A;2711C>G]	ENSP00000344798.4:p.[Val804Met;Ser904Cys]
ENST00000355710.8:c.[2410G>A;2711C>G] MANE Select	ENSP00000347942.3:p.[Val804Met;Ser904Cys]
ENST00000671844.1:c.[*1004G>A;*1305C>G]	ENSP00000500541.1:n.[*1004G>A;*1305C>G]
ENST00000672389.1:c.[*1004G>A;*1305C>G]	ENSP00000500252.1:n.[*1004G>A;*1305C>G]
ENST00000340058.5:c.[2410G>A;2711C>G]	ENSP00000344798.4:p.[Val804Met;Ser904Cys]
ENST00000355710.7:c.[2410G>A;2711C>G]	ENSP00000347942.3:p.[Val804Met;Ser904Cys]
ENST00000615310.4:c.[1290-154G>A;*60C>G]	ENSP00000480088.1:n.[1290-154G>A;*60C>G]
NM_020630.4:c.[2410G>A;2711C>G] , LRG_518t2:c.[2410G>A;2711C>G]	NP_065681.1:p.[Val804Met;Ser904Cys]
NM_020975.4:c.[2410G>A;2711C>G] , LRG_518t1:c.[2410G>A;2711C>G]	NP_066124.1:p.[Val804Met;Ser904Cys]
XM_011540027.1:c.[2410G>A;2711C>G]	XP_011538329.1:p.[Val804Met;Ser904Cys]
NM_001355216.1:c.[1648G>A;1949C>G]	NP_001342145.1:p.[Val550Met;Ser650Cys]
NM_020630.5:c.[2410G>A;2711C>G]	NP_065681.1:p.[Val804Met;Ser904Cys]
NM_020975.5:c.[2410G>A;2711C>G]	NP_066124.1:p.[Val804Met;Ser904Cys]
NM_020975.6:c.[2410G>A;2711C>G] MANE Select	NP_066124.1:p.[Val804Met;Ser904Cys]
NM_020630.6:c.[2410G>A;2711C>G]	NP_065681.1:p.[Val804Met;Ser904Cys]