Canonical Allele Identifier: CA2721859111
Gene: RET HGNC NCBI

Linked Data

dbSNP Id: rs2132661129

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100591del , CM000672.2:g.43100591del GRCh38
NC_000010.10:g.43596039del , CM000672.1:g.43596039del GRCh37
NC_000010.9:g.42916045del NCBI36
NG_007489.1:g.28523del , LRG_518:g.28523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.206del ENSP00000480088.2:p.Gly69AlafsTer?
ENST00000683278.1:c.108del
ENST00000684216.1:c.108del
ENST00000340058.6:c.206del ENSP00000344798.4:p.Gly69AlafsTer?
ENST00000355710.8:c.206del MANE Select ENSP00000347942.3:p.Gly69AlafsTer?
ENST00000638465.1:c.108del
ENST00000640619.1:c.108del
ENST00000671844.1:c.206del ENSP00000500541.1:p.Gly69AlafsTer?
ENST00000672389.1:c.74-10616del ENSP00000500252.1:n.74-10616del
ENST00000340058.5:c.206del ENSP00000344798.4:p.Gly69AlafsTer?
ENST00000355710.7:c.206del ENSP00000347942.3:p.Gly69AlafsTer?
ENST00000498820.5:c.74-11508del ENSP00000419080.1:n.74-11508del
ENST00000615310.4:c.206del ENSP00000480088.1:p.Gly69AlafsTer?
NM_020630.4:c.206del , LRG_518t2:c.206del NP_065681.1:p.Gly69AlafsTer?
NM_020975.4:c.206del , LRG_518t1:c.206del NP_066124.1:p.Gly69AlafsTer?
XM_011540027.1:c.206del XP_011538329.1:p.Gly69AlafsTer?
NM_020630.5:c.206del NP_065681.1:p.Gly69AlafsTer?
NM_020975.5:c.206del NP_066124.1:p.Gly69AlafsTer?
NM_020975.6:c.206del MANE Select NP_066124.1:p.Gly69AlafsTer?
NM_020630.6:c.206del NP_065681.1:p.Gly69AlafsTer?