Canonical Allele Identifier: CA033105

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43111270C>T , CM000672.2:g.43111270C>T	GRCh38
NC_000010.10:g.43606718C>T , CM000672.1:g.43606718C>T	GRCh37
NC_000010.9:g.42926724C>T	NCBI36
NG_007489.1:g.39202C>T , LRG_518:g.39202C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1327C>T MANE Select	NP_066124.1:p.His443Tyr
ENST00000355710.8:c.1327C>T MANE Select	ENSP00000347942.3:p.His443Tyr
NM_001355216.1:c.565C>T	NP_001342145.1:p.His189Tyr
NM_020630.4:c.1327C>T , LRG_518t2:c.1327C>T	NP_065681.1:p.His443Tyr
NM_020630.5:c.1327C>T	NP_065681.1:p.His443Tyr
NM_020630.6:c.1327C>T	NP_065681.1:p.His443Tyr
NM_020975.4:c.1327C>T , LRG_518t1:c.1327C>T	NP_066124.1:p.His443Tyr
NM_020975.5:c.1327C>T	NP_066124.1:p.His443Tyr
ENST00000340058.5:c.1327C>T	ENSP00000344798.4:p.His443Tyr
ENST00000340058.6:c.1327C>T	ENSP00000344798.4:p.His443Tyr
ENST00000355710.7:c.1327C>T	ENSP00000347942.3:p.His443Tyr
ENST00000498820.5:c.74-829C>T	ENSP00000419080.1:n.74-829C>T
ENST00000615310.4:c.1289+38C>T	ENSP00000480088.1:n.1289+38C>T
ENST00000615310.5:c.931C>T	ENSP00000480088.2:p.His311Tyr
ENST00000671844.1:c.689C>T	ENSP00000500541.1:p.Ala230Val
ENST00000672389.1:c.137C>T	ENSP00000500252.1:p.Ala46Val
ENST00000683007.1:n.901C>T
ENST00000683872.1:n.88C>T
XM_011540027.1:c.1327C>T	XP_011538329.1:p.His443Tyr