Canonical Allele Identifier: CA1905809420

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106210T= , CM000672.2:g.43106210T=	GRCh38
NC_000010.10:g.43601658T= , CM000672.1:g.43601658T=	GRCh37
NC_000010.9:g.42921664T=	NCBI36
NG_007489.1:g.34142T= , LRG_518:g.34142T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.867+1017T=	ENSP00000480088.2:n.867+1017T=
ENST00000683007.1:n.442-166T=
ENST00000340058.6:c.868-166T=	ENSP00000344798.4:n.868-166T=
ENST00000355710.8:c.868-166T= MANE Select	ENSP00000347942.3:n.868-166T=
ENST00000671844.1:c.625+3581T=	ENSP00000500541.1:n.625+3581T=
ENST00000672389.1:c.74-4997T=	ENSP00000500252.1:n.74-4997T=
ENST00000340058.5:c.868-166T=	ENSP00000344798.4:n.868-166T=
ENST00000355710.7:c.868-166T=	ENSP00000347942.3:n.868-166T=
ENST00000479913.1:n.463-166T=
ENST00000498820.5:c.74-5889T=	ENSP00000419080.1:n.74-5889T=
ENST00000615310.4:c.868-166T=	ENSP00000480088.1:n.868-166T=
NM_020630.4:c.868-166T= , LRG_518t2:c.868-166T=	NP_065681.1:n.868-166T=
NM_020975.4:c.868-166T= , LRG_518t1:c.868-166T=	NP_066124.1:n.868-166T=
XM_011540027.1:c.868-166T=	XP_011538329.1:n.868-166T=
NM_001355216.1:c.106-166T=	NP_001342145.1:n.106-166T=
NM_020630.5:c.868-166T=	NP_065681.1:n.868-166T=
NM_020975.5:c.868-166T=	NP_066124.1:n.868-166T=
NM_020975.6:c.868-166T= MANE Select	NP_066124.1:n.868-166T=
NM_020630.6:c.868-166T=	NP_065681.1:n.868-166T=