Canonical Allele Identifier: CA1139768700

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43118412_43118413insCTG , CM000672.2:g.43118412_43118413insCTG	GRCh38
NC_000010.10:g.43613860_43613861insCTG , CM000672.1:g.43613860_43613861insCTG	GRCh37
NC_000010.9:g.42933866_42933867insCTG	NCBI36
NG_007489.1:g.46344_46345insCTG , LRG_518:g.46344_46345insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1928_1929insCTG	ENSP00000480088.2:p.Glu643delinsAspTrp
ENST00000683007.1:n.1898_1899insCTG
ENST00000683872.1:n.1889_1890insCTG
ENST00000340058.6:c.2324_2325insCTG	ENSP00000344798.4:p.Glu775delinsAspTrp
ENST00000355710.8:c.2324_2325insCTG MANE Select	ENSP00000347942.3:p.Glu775delinsAspTrp
ENST00000671844.1:c.*918_*919insCTG	ENSP00000500541.1:n.*918_*919insCTG
ENST00000672389.1:c.*918_*919insCTG	ENSP00000500252.1:n.*918_*919insCTG
ENST00000340058.5:c.2324_2325insCTG	ENSP00000344798.4:p.Glu775delinsAspTrp
ENST00000355710.7:c.2324_2325insCTG	ENSP00000347942.3:p.Glu775delinsAspTrp
ENST00000615310.4:c.1290-1290_1290-1289insCTG	ENSP00000480088.1:n.1290-1290_1290-1289insCTG
NM_020630.4:c.2324_2325insCTG , LRG_518t2:c.2324_2325insCTG	NP_065681.1:p.Glu775delinsAspTrp
NM_020975.4:c.2324_2325insCTG , LRG_518t1:c.2324_2325insCTG	NP_066124.1:p.Glu775delinsAspTrp
XM_011540027.1:c.2324_2325insCTG	XP_011538329.1:p.Glu775delinsAspTrp
NM_001355216.1:c.1562_1563insCTG	NP_001342145.1:p.Glu521delinsAspTrp
NM_020630.5:c.2324_2325insCTG	NP_065681.1:p.Glu775delinsAspTrp
NM_020975.5:c.2324_2325insCTG	NP_066124.1:p.Glu775delinsAspTrp
NM_020975.6:c.2324_2325insCTG MANE Select	NP_066124.1:p.Glu775delinsAspTrp
NM_020630.6:c.2324_2325insCTG	NP_065681.1:p.Glu775delinsAspTrp