Canonical Allele Identifier: CA2721926261

Gene: RET

Linked Data

• dbSNP Id: rs2132828897

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43113619_43113624dup , CM000672.2:g.43113619_43113624dup	GRCh38
NC_000010.10:g.43609067_43609072dup , CM000672.1:g.43609067_43609072dup	GRCh37
NC_000010.9:g.42929073_42929078dup	NCBI36
NG_007489.1:g.41551_41556dup , LRG_518:g.41551_41556dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1427_1432dup	ENSP00000480088.2:p.Cys477_Asn478insThrCys
ENST00000683007.1:n.1397_1402dup
ENST00000683872.1:n.584_589dup
ENST00000340058.6:c.1823_1828dup	ENSP00000344798.4:p.Cys609_Asn610insThrCys
ENST00000355710.8:c.1823_1828dup MANE Select	ENSP00000347942.3:p.Cys609_Asn610insThrCys
ENST00000671844.1:c.*417_*422dup	ENSP00000500541.1:n.*417_*422dup
ENST00000672389.1:c.*417_*422dup	ENSP00000500252.1:n.*417_*422dup
ENST00000340058.5:c.1823_1828dup	ENSP00000344798.4:p.Cys609_Asn610insThrCys
ENST00000355710.7:c.1823_1828dup	ENSP00000347942.3:p.Cys609_Asn610insThrCys
ENST00000498820.5:c.374_379dup	ENSP00000419080.1:p.Cys126_Asn127insThrCys
ENST00000615310.4:c.1289+2387_1289+2392dup	ENSP00000480088.1:n.1289+2387_1289+2392dup
NM_020630.4:c.1823_1828dup , LRG_518t2:c.1823_1828dup	NP_065681.1:p.Cys609_Asn610insThrCys
NM_020975.4:c.1823_1828dup , LRG_518t1:c.1823_1828dup	NP_066124.1:p.Cys609_Asn610insThrCys
XM_011540027.1:c.1823_1828dup	XP_011538329.1:p.Cys609_Asn610insThrCys
NM_001355216.1:c.1061_1066dup	NP_001342145.1:p.Cys355_Asn356insThrCys
NM_020630.5:c.1823_1828dup	NP_065681.1:p.Cys609_Asn610insThrCys
NM_020975.5:c.1823_1828dup	NP_066124.1:p.Cys609_Asn610insThrCys
NM_020975.6:c.1823_1828dup MANE Select	NP_066124.1:p.Cys609_Asn610insThrCys
NM_020630.6:c.1823_1828dup	NP_065681.1:p.Cys609_Asn610insThrCys