Canonical Allele Identifier: CA16612889

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120162C>T , CM000672.2:g.43120162C>T	GRCh38
NC_000010.10:g.43615610C>T , CM000672.1:g.43615610C>T	GRCh37
NC_000010.9:g.42935616C>T	NCBI36
NG_007489.1:g.48094C>T , LRG_518:g.48094C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2293C>T	ENSP00000480088.2:p.Arg765Ter
ENST00000683007.1:n.2263C>T
ENST00000683872.1:n.2254C>T
ENST00000340058.6:c.2689C>T	ENSP00000344798.4:p.Arg897Ter
ENST00000355710.8:c.2689C>T MANE Select	ENSP00000347942.3:p.Arg897Ter
ENST00000671844.1:c.*1283C>T	ENSP00000500541.1:n.*1283C>T
ENST00000672389.1:c.*1283C>T	ENSP00000500252.1:n.*1283C>T
ENST00000340058.5:c.2689C>T	ENSP00000344798.4:p.Arg897Ter
ENST00000355710.7:c.2689C>T	ENSP00000347942.3:p.Arg897Ter
ENST00000615310.4:c.*38C>T	ENSP00000480088.1:n.*38C>T
NM_020630.4:c.2689C>T , LRG_518t2:c.2689C>T	NP_065681.1:p.Arg897Ter
NM_020975.4:c.2689C>T , LRG_518t1:c.2689C>T	NP_066124.1:p.Arg897Ter
XM_011540027.1:c.2689C>T	XP_011538329.1:p.Arg897Ter
NM_001355216.1:c.1927C>T	NP_001342145.1:p.Arg643Ter
NM_020630.5:c.2689C>T	NP_065681.1:p.Arg897Ter
NM_020975.5:c.2689C>T	NP_066124.1:p.Arg897Ter
NM_020975.6:c.2689C>T MANE Select	NP_066124.1:p.Arg897Ter
NM_020630.6:c.2689C>T	NP_065681.1:p.Arg897Ter