Canonical Allele Identifier: CA1905809497

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106393G= , CM000672.2:g.43106393G=	GRCh38
NC_000010.10:g.43601841G= , CM000672.1:g.43601841G=	GRCh37
NC_000010.9:g.42921847G=	NCBI36
NG_007489.1:g.34325G= , LRG_518:g.34325G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.867+1200G=	ENSP00000480088.2:n.867+1200G=
ENST00000683007.1:n.459G=
ENST00000340058.6:c.885G=	ENSP00000344798.4:p.Thr295=
ENST00000355710.8:c.885G= MANE Select	ENSP00000347942.3:p.Thr295=
ENST00000671844.1:c.625+3764G=	ENSP00000500541.1:n.625+3764G=
ENST00000672389.1:c.74-4814G=	ENSP00000500252.1:n.74-4814G=
ENST00000340058.5:c.885G=	ENSP00000344798.4:p.Thr295=
ENST00000355710.7:c.885G=	ENSP00000347942.3:p.Thr295=
ENST00000479913.1:n.480G=
ENST00000498820.5:c.74-5706G=	ENSP00000419080.1:n.74-5706G=
ENST00000615310.4:c.885G=	ENSP00000480088.1:p.Thr295=
NM_020630.4:c.885G= , LRG_518t2:c.885G=	NP_065681.1:p.Thr295=
NM_020975.4:c.885G= , LRG_518t1:c.885G=	NP_066124.1:p.Thr295=
XM_011540027.1:c.885G=	XP_011538329.1:p.Thr295=
NM_001355216.1:c.123G=	NP_001342145.1:p.Thr41=
NM_020630.5:c.885G=	NP_065681.1:p.Thr295=
NM_020975.5:c.885G=	NP_066124.1:p.Thr295=
NM_020975.6:c.885G= MANE Select	NP_066124.1:p.Thr295=
NM_020630.6:c.885G=	NP_065681.1:p.Thr295=