Canonical Allele Identifier: CA2840894650

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113599dup , CM000672.2:g.43113599dup	GRCh38
NC_000010.10:g.43609047dup , CM000672.1:g.43609047dup	GRCh37
NC_000010.9:g.42929053dup	NCBI36
NG_007489.1:g.41531dup , LRG_518:g.41531dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.1407dup	ENSP00000480088.2:p.Ile470AspfsTer2
ENST00000683007.1:n.1377dup
ENST00000683872.1:n.564dup
ENST00000340058.6:c.1803dup	ENSP00000344798.4:p.Ile602AspfsTer2
ENST00000355710.8:c.1803dup MANE Select	ENSP00000347942.3:p.Ile602AspfsTer2
ENST00000671844.1:c.*397dup	ENSP00000500541.1:n.*397dup
ENST00000672389.1:c.*397dup	ENSP00000500252.1:n.*397dup
ENST00000340058.5:c.1803dup	ENSP00000344798.4:p.Ile602AspfsTer2
ENST00000355710.7:c.1803dup	ENSP00000347942.3:p.Ile602AspfsTer2
ENST00000498820.5:c.354dup	ENSP00000419080.1:p.Ile119AspfsTer2
ENST00000615310.4:c.1289+2367dup	ENSP00000480088.1:n.1289+2367dup
NM_020630.4:c.1803dup , LRG_518t2:c.1803dup	NP_065681.1:p.Ile602AspfsTer2
NM_020975.4:c.1803dup , LRG_518t1:c.1803dup	NP_066124.1:p.Ile602AspfsTer2
XM_011540027.1:c.1803dup	XP_011538329.1:p.Ile602AspfsTer2
NM_001355216.1:c.1041dup	NP_001342145.1:p.Ile348AspfsTer2
NM_020630.5:c.1803dup	NP_065681.1:p.Ile602AspfsTer2
NM_020975.5:c.1803dup	NP_066124.1:p.Ile602AspfsTer2
NM_020975.6:c.1803dup MANE Select	NP_066124.1:p.Ile602AspfsTer2
NM_020630.6:c.1803dup	NP_065681.1:p.Ile602AspfsTer2