Canonical Allele Identifier: CA2841991399

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43119607dup , CM000672.2:g.43119607dup	GRCh38
NC_000010.10:g.43615055dup , CM000672.1:g.43615055dup	GRCh37
NC_000010.9:g.42935061dup	NCBI36
NG_007489.1:g.47539dup , LRG_518:g.47539dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2073dup	ENSP00000480088.2:p.Pro692AlafsTer20
ENST00000683007.1:n.2043dup
ENST00000683872.1:n.2034dup
ENST00000340058.6:c.2469dup	ENSP00000344798.4:p.Pro824AlafsTer20
ENST00000355710.8:c.2469dup MANE Select	ENSP00000347942.3:p.Pro824AlafsTer20
ENST00000671844.1:c.*1063dup	ENSP00000500541.1:n.*1063dup
ENST00000672389.1:c.*1063dup	ENSP00000500252.1:n.*1063dup
ENST00000340058.5:c.2469dup	ENSP00000344798.4:p.Pro824AlafsTer20
ENST00000355710.7:c.2469dup	ENSP00000347942.3:p.Pro824AlafsTer20
ENST00000615310.4:c.1290-95dup	ENSP00000480088.1:n.1290-95dup
NM_020630.4:c.2469dup , LRG_518t2:c.2469dup	NP_065681.1:p.Pro824AlafsTer20
NM_020975.4:c.2469dup , LRG_518t1:c.2469dup	NP_066124.1:p.Pro824AlafsTer20
XM_011540027.1:c.2469dup	XP_011538329.1:p.Pro824AlafsTer20
NM_001355216.1:c.1707dup	NP_001342145.1:p.Pro570AlafsTer20
NM_020630.5:c.2469dup	NP_065681.1:p.Pro824AlafsTer20
NM_020975.5:c.2469dup	NP_066124.1:p.Pro824AlafsTer20
NM_020975.6:c.2469dup MANE Select	NP_066124.1:p.Pro824AlafsTer20
NM_020630.6:c.2469dup	NP_065681.1:p.Pro824AlafsTer20