Canonical Allele Identifier: CA1905813061

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113629C= , CM000672.2:g.43113629C=	GRCh38
NC_000010.10:g.43609077C= , CM000672.1:g.43609077C=	GRCh37
NC_000010.9:g.42929083C=	NCBI36
NG_007489.1:g.41561C= , LRG_518:g.41561C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1437C=	ENSP00000480088.2:p.Cys479=
ENST00000683007.1:n.1407C=
ENST00000683872.1:n.594C=
ENST00000340058.6:c.1833C=	ENSP00000344798.4:p.Cys611=
ENST00000355710.8:c.1833C= MANE Select	ENSP00000347942.3:p.Cys611=
ENST00000671844.1:c.*427C=	ENSP00000500541.1:n.*427C=
ENST00000672389.1:c.*427C=	ENSP00000500252.1:n.*427C=
ENST00000340058.5:c.1833C=	ENSP00000344798.4:p.Cys611=
ENST00000355710.7:c.1833C=	ENSP00000347942.3:p.Cys611=
ENST00000498820.5:c.384C=	ENSP00000419080.1:p.Cys128=
ENST00000615310.4:c.1289+2397C=	ENSP00000480088.1:n.1289+2397C=
NM_020630.4:c.1833C= , LRG_518t2:c.1833C=	NP_065681.1:p.Cys611=
NM_020975.4:c.1833C= , LRG_518t1:c.1833C=	NP_066124.1:p.Cys611=
XM_011540027.1:c.1833C=	XP_011538329.1:p.Cys611=
NM_001355216.1:c.1071C=	NP_001342145.1:p.Cys357=
NM_020630.5:c.1833C=	NP_065681.1:p.Cys611=
NM_020975.5:c.1833C=	NP_066124.1:p.Cys611=
NM_020975.6:c.1833C= MANE Select	NP_066124.1:p.Cys611=
NM_020630.6:c.1833C=	NP_065681.1:p.Cys611=