Canonical Allele Identifier: CA2608894522
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100786_43100787del , CM000672.2:g.43100786_43100787del GRCh38
NC_000010.10:g.43596234_43596235del , CM000672.1:g.43596234_43596235del GRCh37
NC_000010.9:g.42916240_42916241del NCBI36
NG_007489.1:g.28718_28719del , LRG_518:g.28718_28719del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.337+64_337+65del ENSP00000480088.2:n.337+64_337+65del
ENST00000683278.1:c.239+64_239+65del
ENST00000684216.1:c.239+64_239+65del
ENST00000340058.6:c.337+64_337+65del ENSP00000344798.4:n.337+64_337+65del
ENST00000355710.8:c.337+64_337+65del MANE Select ENSP00000347942.3:n.337+64_337+65del
ENST00000638465.1:c.239+64_239+65del
ENST00000640619.1:c.239+64_239+65del
ENST00000671844.1:c.337+64_337+65del ENSP00000500541.1:n.337+64_337+65del
ENST00000672389.1:c.74-10421_74-10420del ENSP00000500252.1:n.74-10421_74-10420del
ENST00000340058.5:c.337+64_337+65del ENSP00000344798.4:n.337+64_337+65del
ENST00000355710.7:c.337+64_337+65del ENSP00000347942.3:n.337+64_337+65del
ENST00000498820.5:c.74-11313_74-11312del ENSP00000419080.1:n.74-11313_74-11312del
ENST00000615310.4:c.337+64_337+65del ENSP00000480088.1:n.337+64_337+65del
NM_020630.4:c.337+64_337+65del , LRG_518t2:c.337+64_337+65del NP_065681.1:n.337+64_337+65del
NM_020975.4:c.337+64_337+65del , LRG_518t1:c.337+64_337+65del NP_066124.1:n.337+64_337+65del
XM_011540027.1:c.337+64_337+65del XP_011538329.1:n.337+64_337+65del
NM_020630.5:c.337+64_337+65del NP_065681.1:n.337+64_337+65del
NM_020975.5:c.337+64_337+65del NP_066124.1:n.337+64_337+65del
NM_020975.6:c.337+64_337+65del MANE Select NP_066124.1:n.337+64_337+65del
NM_020630.6:c.337+64_337+65del NP_065681.1:n.337+64_337+65del