Canonical Allele Identifier: CA2841991397
Gene: RET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43119585del , CM000672.2:g.43119585del GRCh38
NC_000010.10:g.43615033del , CM000672.1:g.43615033del GRCh37
NC_000010.9:g.42935039del NCBI36
NG_007489.1:g.47517del , LRG_518:g.47517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.2051del ENSP00000480088.2:p.Leu684ProfsTer?
ENST00000683007.1:n.2021del
ENST00000683872.1:n.2012del
ENST00000340058.6:c.2447del ENSP00000344798.4:p.Leu816ProfsTer?
ENST00000355710.8:c.2447del MANE Select ENSP00000347942.3:p.Leu816ProfsTer?
ENST00000671844.1:c.*1041del ENSP00000500541.1:n.*1041del
ENST00000672389.1:c.*1041del ENSP00000500252.1:n.*1041del
ENST00000340058.5:c.2447del ENSP00000344798.4:p.Leu816ProfsTer?
ENST00000355710.7:c.2447del ENSP00000347942.3:p.Leu816ProfsTer?
ENST00000615310.4:c.1290-117del ENSP00000480088.1:n.1290-117del
NM_020630.4:c.2447del , LRG_518t2:c.2447del NP_065681.1:p.Leu816ProfsTer?
NM_020975.4:c.2447del , LRG_518t1:c.2447del NP_066124.1:p.Leu816ProfsTer?
XM_011540027.1:c.2447del XP_011538329.1:p.Leu816ProfsTer?
NM_001355216.1:c.1685del NP_001342145.1:p.Leu562ProfsTer?
NM_020630.5:c.2447del NP_065681.1:p.Leu816ProfsTer?
NM_020975.5:c.2447del NP_066124.1:p.Leu816ProfsTer?
NM_020975.6:c.2447del MANE Select NP_066124.1:p.Leu816ProfsTer?
NM_020630.6:c.2447del NP_065681.1:p.Leu816ProfsTer?