Canonical Allele Identifier: CA1905813052

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113621T= , CM000672.2:g.43113621T=	GRCh38
NC_000010.10:g.43609069T= , CM000672.1:g.43609069T=	GRCh37
NC_000010.9:g.42929075T=	NCBI36
NG_007489.1:g.41553T= , LRG_518:g.41553T=

Transcript Alleles

HGVS	Amino-acid Change
NM_020975.6:c.1825T= MANE Select	NP_066124.1:p.Cys609=
ENST00000355710.8:c.1825T= MANE Select	ENSP00000347942.3:p.Cys609=
NM_001355216.1:c.1063T=	NP_001342145.1:p.Cys355=
NM_020630.4:c.1825T= , LRG_518t2:c.1825T=	NP_065681.1:p.Cys609=
NM_020630.5:c.1825T=	NP_065681.1:p.Cys609=
NM_020630.6:c.1825T=	NP_065681.1:p.Cys609=
NM_020975.4:c.1825T= , LRG_518t1:c.1825T=	NP_066124.1:p.Cys609=
NM_020975.5:c.1825T=	NP_066124.1:p.Cys609=
ENST00000340058.5:c.1825T=	ENSP00000344798.4:p.Cys609=
ENST00000340058.6:c.1825T=	ENSP00000344798.4:p.Cys609=
ENST00000355710.7:c.1825T=	ENSP00000347942.3:p.Cys609=
ENST00000498820.5:c.376T=	ENSP00000419080.1:p.Cys126=
ENST00000615310.4:c.1289+2389T=	ENSP00000480088.1:n.1289+2389T=
ENST00000615310.5:c.1429T=	ENSP00000480088.2:p.Cys477=
ENST00000671844.1:c.*419T=	ENSP00000500541.1:n.*419T=
ENST00000672389.1:c.*419T=	ENSP00000500252.1:n.*419T=
ENST00000683007.1:n.1399T=
ENST00000683872.1:n.586T=
XM_011540027.1:c.1825T=	XP_011538329.1:p.Cys609=