Canonical Allele Identifier: CA1905813457

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114489_43114492delinsGCGA , CM000672.2:g.43114489_43114492delinsGCGA	GRCh38
NC_000010.10:g.43609937_43609940delinsGCGA , CM000672.1:g.43609937_43609940delinsGCGA	GRCh37
NC_000010.9:g.42929943_42929946delinsGCGA	NCBI36
NG_007489.1:g.42421_42424delinsGCGA , LRG_518:g.42421_42424delinsGCGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1493_1496delinsGCGA	ENSP00000480088.2:p.Cys498=
ENST00000683007.1:n.1463_1466delinsGCGA
ENST00000683872.1:n.1454_1457delinsGCGA
ENST00000340058.6:c.1889_1892delinsGCGA	ENSP00000344798.4:p.Cys630=
ENST00000355710.8:c.1889_1892delinsGCGA MANE Select	ENSP00000347942.3:p.Cys630=
ENST00000671844.1:c.*483_*486delinsGCGA	ENSP00000500541.1:n.*483_*486delinsGCGA
ENST00000672389.1:c.*483_*486delinsGCGA	ENSP00000500252.1:n.*483_*486delinsGCGA
ENST00000340058.5:c.1889_1892delinsGCGA	ENSP00000344798.4:p.Cys630=
ENST00000355710.7:c.1889_1892delinsGCGA	ENSP00000347942.3:p.Cys630=
ENST00000498820.5:c.440_443delinsGCGA	ENSP00000419080.1:p.Cys147=
ENST00000615310.4:c.1289+3257_1289+3260delinsGCGA	ENSP00000480088.1:n.1289+3257_1289+3260delinsGCGA
NM_020630.4:c.1889_1892delinsGCGA , LRG_518t2:c.1889_1892delinsGCGA	NP_065681.1:p.Cys630=
NM_020975.4:c.1889_1892delinsGCGA , LRG_518t1:c.1889_1892delinsGCGA	NP_066124.1:p.Cys630=
XM_011540027.1:c.1889_1892delinsGCGA	XP_011538329.1:p.Cys630=
NM_001355216.1:c.1127_1130delinsGCGA	NP_001342145.1:p.Cys376=
NM_020630.5:c.1889_1892delinsGCGA	NP_065681.1:p.Cys630=
NM_020975.5:c.1889_1892delinsGCGA	NP_066124.1:p.Cys630=
NM_020975.6:c.1889_1892delinsGCGA MANE Select	NP_066124.1:p.Cys630=
NM_020630.6:c.1889_1892delinsGCGA	NP_065681.1:p.Cys630=