Canonical Allele Identifier: CA1905813469

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114496_43114497delinsGC , CM000672.2:g.43114496_43114497delinsGC	GRCh38
NC_000010.10:g.43609944_43609945delinsGC , CM000672.1:g.43609944_43609945delinsGC	GRCh37
NC_000010.9:g.42929950_42929951delinsGC	NCBI36
NG_007489.1:g.42428_42429delinsGC , LRG_518:g.42428_42429delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1500_1501delinsGC	ENSP00000480088.2:p.Glu500=
ENST00000683007.1:n.1470_1471delinsGC
ENST00000683872.1:n.1461_1462delinsGC
ENST00000340058.6:c.1896_1897delinsGC	ENSP00000344798.4:p.Glu632=
ENST00000355710.8:c.1896_1897delinsGC MANE Select	ENSP00000347942.3:p.Glu632=
ENST00000671844.1:c.*490_*491delinsGC	ENSP00000500541.1:n.*490_*491delinsGC
ENST00000672389.1:c.*490_*491delinsGC	ENSP00000500252.1:n.*490_*491delinsGC
ENST00000340058.5:c.1896_1897delinsGC	ENSP00000344798.4:p.Glu632=
ENST00000355710.7:c.1896_1897delinsGC	ENSP00000347942.3:p.Glu632=
ENST00000498820.5:c.447_448delinsGC	ENSP00000419080.1:p.Glu149=
ENST00000615310.4:c.1289+3264_1289+3265delinsGC	ENSP00000480088.1:n.1289+3264_1289+3265delinsGC
NM_020630.4:c.1896_1897delinsGC , LRG_518t2:c.1896_1897delinsGC	NP_065681.1:p.Glu632=
NM_020975.4:c.1896_1897delinsGC , LRG_518t1:c.1896_1897delinsGC	NP_066124.1:p.Glu632=
XM_011540027.1:c.1896_1897delinsGC	XP_011538329.1:p.Glu632=
NM_001355216.1:c.1134_1135delinsGC	NP_001342145.1:p.Glu378=
NM_020630.5:c.1896_1897delinsGC	NP_065681.1:p.Glu632=
NM_020975.5:c.1896_1897delinsGC	NP_066124.1:p.Glu632=
NM_020975.6:c.1896_1897delinsGC MANE Select	NP_066124.1:p.Glu632=
NM_020630.6:c.1896_1897delinsGC	NP_065681.1:p.Glu632=