Canonical Allele Identifier: CA1139659388

Gene: RET

Linked Data

• ClinVar Variation Id: 932072
• ClinVar RCV Id: RCV001199205
• dbSNP Id: rs1838178970

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43120104del , CM000672.2:g.43120104del	GRCh38
NC_000010.10:g.43615552del , CM000672.1:g.43615552del	GRCh37
NC_000010.9:g.42935558del	NCBI36
NG_007489.1:g.48036del , LRG_518:g.48036del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.2235del	ENSP00000480088.2:p.Arg746GlufsTer5
ENST00000683007.1:n.2205del
ENST00000683872.1:n.2196del
ENST00000340058.6:c.2631del	ENSP00000344798.4:p.Arg878GlufsTer5
ENST00000355710.8:c.2631del MANE Select	ENSP00000347942.3:p.Arg878GlufsTer5
ENST00000671844.1:c.*1225del	ENSP00000500541.1:n.*1225del
ENST00000672389.1:c.*1225del	ENSP00000500252.1:n.*1225del
ENST00000340058.5:c.2631del	ENSP00000344798.4:p.Arg878GlufsTer5
ENST00000355710.7:c.2631del	ENSP00000347942.3:p.Arg878GlufsTer5
ENST00000615310.4:c.1357del	ENSP00000480088.1:p.Gln453ArgfsTer?
NM_020630.4:c.2631del , LRG_518t2:c.2631del	NP_065681.1:p.Arg878GlufsTer5
NM_020975.4:c.2631del , LRG_518t1:c.2631del	NP_066124.1:p.Arg878GlufsTer5
XM_011540027.1:c.2631del	XP_011538329.1:p.Arg878GlufsTer5
NM_001355216.1:c.1869del	NP_001342145.1:p.Arg624GlufsTer5
NM_020630.5:c.2631del	NP_065681.1:p.Arg878GlufsTer5
NM_020975.5:c.2631del	NP_066124.1:p.Arg878GlufsTer5
NM_020975.6:c.2631del MANE Select	NP_066124.1:p.Arg878GlufsTer5
NM_020630.6:c.2631del	NP_065681.1:p.Arg878GlufsTer5