Canonical Allele Identifier: CA645541248

Gene: RET

Linked Data

• COSMIC: COSM86006

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114492_43114514delinsCG , CM000672.2:g.43114492_43114514delinsCG	GRCh38
NC_000010.10:g.43609940_43609962delinsCG , CM000672.1:g.43609940_43609962delinsCG	GRCh37
NC_000010.9:g.42929946_42929968delinsCG	NCBI36
NG_007489.1:g.42424_42446delinsCG , LRG_518:g.42424_42446delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1496_1518delinsCG	ENSP00000480088.2:p.Asp499_Ile506delinsAl...
ENST00000683007.1:n.1466_1488delinsCG
ENST00000683872.1:n.1457_1479delinsCG
ENST00000340058.6:c.1892_1914delinsCG	ENSP00000344798.4:p.Asp631_Ile638delinsAl...
ENST00000355710.8:c.1892_1914delinsCG MANE Select	ENSP00000347942.3:p.Asp631_Ile638delinsAl...
ENST00000671844.1:c.*486_*508delinsCG	ENSP00000500541.1:n.*486_*508delinsCG
ENST00000672389.1:c.*486_*508delinsCG	ENSP00000500252.1:n.*486_*508delinsCG
ENST00000340058.5:c.1892_1914delinsCG	ENSP00000344798.4:p.Asp631_Ile638delinsAl...
ENST00000355710.7:c.1892_1914delinsCG	ENSP00000347942.3:p.Asp631_Ile638delinsAl...
ENST00000498820.5:c.443_465delinsCG	ENSP00000419080.1:p.Asp148_Ile155delinsAl...
ENST00000615310.4:c.1289+3260_1289+3282delinsCG	ENSP00000480088.1:n.1289+3260_1289+3282de...
NM_020630.4:c.1892_1914delinsCG , LRG_518t2:c.1892_1914delinsCG	NP_065681.1:p.Asp631_Ile638delinsAla
NM_020975.4:c.1892_1914delinsCG , LRG_518t1:c.1892_1914delinsCG	NP_066124.1:p.Asp631_Ile638delinsAla
XM_011540027.1:c.1892_1914delinsCG	XP_011538329.1:p.Asp631_Ile638delinsAla
NM_001355216.1:c.1130_1152delinsCG	NP_001342145.1:p.Asp377_Ile384delinsAla
NM_020630.5:c.1892_1914delinsCG	NP_065681.1:p.Asp631_Ile638delinsAla
NM_020975.5:c.1892_1914delinsCG	NP_066124.1:p.Asp631_Ile638delinsAla
NM_020975.6:c.1892_1914delinsCG MANE Select	NP_066124.1:p.Asp631_Ile638delinsAla
NM_020630.6:c.1892_1914delinsCG	NP_065681.1:p.Asp631_Ile638delinsAla