Canonical Allele Identifier: CA645541252

Gene: RET

Linked Data

• dbSNP Id: rs2132844137
• COSMIC: COSM973

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43114495_43114500del , CM000672.2:g.43114495_43114500del	GRCh38
NC_000010.10:g.43609943_43609948del , CM000672.1:g.43609943_43609948del	GRCh37
NC_000010.9:g.42929949_42929954del	NCBI36
NG_007489.1:g.42427_42432del , LRG_518:g.42427_42432del

Transcript Alleles

HGVS	Amino-acid change
ENST00000615310.5:c.1499_1504del	ENSP00000480088.2:p.Glu500_Cys502delinsGly
ENST00000683007.1:n.1469_1474del
ENST00000683872.1:n.1460_1465del
ENST00000340058.6:c.1895_1900del	ENSP00000344798.4:p.Glu632_Cys634delinsGly
ENST00000355710.8:c.1895_1900del MANE Select	ENSP00000347942.3:p.Glu632_Cys634delinsGly
ENST00000671844.1:c.*489_*494del	ENSP00000500541.1:n.*489_*494del
ENST00000672389.1:c.*489_*494del	ENSP00000500252.1:n.*489_*494del
ENST00000340058.5:c.1895_1900del	ENSP00000344798.4:p.Glu632_Cys634delinsGly
ENST00000355710.7:c.1895_1900del	ENSP00000347942.3:p.Glu632_Cys634delinsGly
ENST00000498820.5:c.446_451del	ENSP00000419080.1:p.Glu149_Cys151delinsGly
ENST00000615310.4:c.1289+3263_1289+3268del	ENSP00000480088.1:n.1289+3263_1289+3268del
NM_020630.4:c.1895_1900del , LRG_518t2:c.1895_1900del	NP_065681.1:p.Glu632_Cys634delinsGly
NM_020975.4:c.1895_1900del , LRG_518t1:c.1895_1900del	NP_066124.1:p.Glu632_Cys634delinsGly
XM_011540027.1:c.1895_1900del	XP_011538329.1:p.Glu632_Cys634delinsGly
NM_001355216.1:c.1133_1138del	NP_001342145.1:p.Glu378_Cys380delinsGly
NM_020630.5:c.1895_1900del	NP_065681.1:p.Glu632_Cys634delinsGly
NM_020975.5:c.1895_1900del	NP_066124.1:p.Glu632_Cys634delinsGly
NM_020975.6:c.1895_1900del MANE Select	NP_066124.1:p.Glu632_Cys634delinsGly
NM_020630.6:c.1895_1900del	NP_065681.1:p.Glu632_Cys634delinsGly