Canonical Allele Identifier: CA2580081456
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2447524

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43077260_43077265dup , CM000672.2:g.43077260_43077265dup GRCh38
NC_000010.10:g.43572708_43572713dup , CM000672.1:g.43572708_43572713dup GRCh37
NC_000010.9:g.42892714_42892719dup NCBI36
NG_007489.1:g.5192_5197dup , LRG_518:g.5192_5197dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2_7dup ENSP00000480088.2:p.Ala2_Lys3insMetAla
ENST00000340058.6:c.2_7dup ENSP00000344798.4:p.Ala2_Lys3insMetAla
ENST00000355710.8:c.2_7dup MANE Select ENSP00000347942.3:p.Ala2_Lys3insMetAla
ENST00000671844.1:c.2_7dup ENSP00000500541.1:p.Ala2_Lys3insMetAla
ENST00000672389.1:c.2_7dup ENSP00000500252.1:p.Ala2_Lys3insMetAla
ENST00000340058.5:c.2_7dup ENSP00000344798.4:p.Ala2_Lys3insMetAla
ENST00000355710.7:c.2_7dup ENSP00000347942.3:p.Ala2_Lys3insMetAla
ENST00000498820.5:c.2_7dup ENSP00000419080.1:p.Ala2_Lys3insMetAla
ENST00000615310.4:c.2_7dup ENSP00000480088.1:p.Ala2_Lys3insMetAla
NM_020630.4:c.2_7dup , LRG_518t2:c.2_7dup NP_065681.1:p.Ala2_Lys3insMetAla
NM_020975.4:c.2_7dup , LRG_518t1:c.2_7dup NP_066124.1:p.Ala2_Lys3insMetAla
XM_011540027.1:c.2_7dup XP_011538329.1:p.Ala2_Lys3insMetAla
NM_020630.5:c.2_7dup NP_065681.1:p.Ala2_Lys3insMetAla
NM_020975.5:c.2_7dup NP_066124.1:p.Ala2_Lys3insMetAla
NM_020975.6:c.2_7dup MANE Select NP_066124.1:p.Ala2_Lys3insMetAla
NM_020630.6:c.2_7dup NP_065681.1:p.Ala2_Lys3insMetAla