Canonical Allele Identifier: CA2840894649

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113594del , CM000672.2:g.43113594del	GRCh38
NC_000010.10:g.43609042del , CM000672.1:g.43609042del	GRCh37
NC_000010.9:g.42929048del	NCBI36
NG_007489.1:g.41526del , LRG_518:g.41526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1402del	ENSP00000480088.2:p.Arg468GlyfsTer?
ENST00000683007.1:n.1372del
ENST00000683872.1:n.559del
ENST00000340058.6:c.1798del	ENSP00000344798.4:p.Arg600GlyfsTer?
ENST00000355710.8:c.1798del MANE Select	ENSP00000347942.3:p.Arg600GlyfsTer?
ENST00000671844.1:c.*392del	ENSP00000500541.1:n.*392del
ENST00000672389.1:c.*392del	ENSP00000500252.1:n.*392del
ENST00000340058.5:c.1798del	ENSP00000344798.4:p.Arg600GlyfsTer?
ENST00000355710.7:c.1798del	ENSP00000347942.3:p.Arg600GlyfsTer?
ENST00000498820.5:c.349del	ENSP00000419080.1:p.Arg117GlyfsTer?
ENST00000615310.4:c.1289+2362del	ENSP00000480088.1:n.1289+2362del
NM_020630.4:c.1798del , LRG_518t2:c.1798del	NP_065681.1:p.Arg600GlyfsTer?
NM_020975.4:c.1798del , LRG_518t1:c.1798del	NP_066124.1:p.Arg600GlyfsTer?
XM_011540027.1:c.1798del	XP_011538329.1:p.Arg600GlyfsTer?
NM_001355216.1:c.1036del	NP_001342145.1:p.Arg346GlyfsTer?
NM_020630.5:c.1798del	NP_065681.1:p.Arg600GlyfsTer?
NM_020975.5:c.1798del	NP_066124.1:p.Arg600GlyfsTer?
NM_020975.6:c.1798del MANE Select	NP_066124.1:p.Arg600GlyfsTer?
NM_020630.6:c.1798del	NP_065681.1:p.Arg600GlyfsTer?