Canonical Allele Identifier: CA665315406

Gene: RET

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43127485T>A , CM000672.2:g.43127485T>A	GRCh38
NC_000010.10:g.43622933T>A , CM000672.1:g.43622933T>A	GRCh37
NC_000010.9:g.42942939T>A	NCBI36
NG_007489.1:g.55417T>A , LRG_518:g.55417T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*731T>A	ENSP00000480088.2:n.*731T>A
ENST00000683007.1:n.3524T>A
ENST00000340058.6:c.*731T>A	ENSP00000344798.4:n.*731T>A
ENST00000355710.8:c.3188-627T>A MANE Select	ENSP00000347942.3:n.3188-627T>A
ENST00000340058.5:c.*731T>A	ENSP00000344798.4:n.*731T>A
ENST00000355710.7:c.3188-627T>A	ENSP00000347942.3:n.3188-627T>A
ENST00000615310.4:c.*537-627T>A	ENSP00000480088.1:n.*537-627T>A
NM_020630.4:c.*731T>A , LRG_518t2:c.*731T>A	NP_065681.1:n.*731T>A
NM_020975.4:c.3188-627T>A , LRG_518t1:c.3188-627T>A	NP_066124.1:n.3188-627T>A
XM_011540027.1:c.3188-627T>A	XP_011538329.1:n.3188-627T>A
NM_001355216.1:c.*731T>A	NP_001342145.1:n.*731T>A
NM_020630.5:c.*731T>A	NP_065681.1:n.*731T>A
NM_020975.5:c.3188-627T>A	NP_066124.1:n.3188-627T>A
NM_020975.6:c.3188-627T>A MANE Select	NP_066124.1:n.3188-627T>A
NM_020630.6:c.*731T>A	NP_065681.1:n.*731T>A