Canonical Allele Identifier: CA2608894515
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100780_43100790del , CM000672.2:g.43100780_43100790del GRCh38
NC_000010.10:g.43596228_43596238del , CM000672.1:g.43596228_43596238del GRCh37
NC_000010.9:g.42916234_42916244del NCBI36
NG_007489.1:g.28712_28722del , LRG_518:g.28712_28722del

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.337+58_337+68del ENSP00000480088.2:n.337+58_337+68del
ENST00000683278.1:c.239+58_239+68del
ENST00000684216.1:c.239+58_239+68del
ENST00000340058.6:c.337+58_337+68del ENSP00000344798.4:n.337+58_337+68del
ENST00000355710.8:c.337+58_337+68del MANE Select ENSP00000347942.3:n.337+58_337+68del
ENST00000638465.1:c.239+58_239+68del
ENST00000640619.1:c.239+58_239+68del
ENST00000671844.1:c.337+58_337+68del ENSP00000500541.1:n.337+58_337+68del
ENST00000672389.1:c.74-10427_74-10417del ENSP00000500252.1:n.74-10427_74-10417del
ENST00000340058.5:c.337+58_337+68del ENSP00000344798.4:n.337+58_337+68del
ENST00000355710.7:c.337+58_337+68del ENSP00000347942.3:n.337+58_337+68del
ENST00000498820.5:c.74-11319_74-11309del ENSP00000419080.1:n.74-11319_74-11309del
ENST00000615310.4:c.337+58_337+68del ENSP00000480088.1:n.337+58_337+68del
NM_020630.4:c.337+58_337+68del , LRG_518t2:c.337+58_337+68del NP_065681.1:n.337+58_337+68del
NM_020975.4:c.337+58_337+68del , LRG_518t1:c.337+58_337+68del NP_066124.1:n.337+58_337+68del
XM_011540027.1:c.337+58_337+68del XP_011538329.1:n.337+58_337+68del
NM_020630.5:c.337+58_337+68del NP_065681.1:n.337+58_337+68del
NM_020975.5:c.337+58_337+68del NP_066124.1:n.337+58_337+68del
NM_020975.6:c.337+58_337+68del MANE Select NP_066124.1:n.337+58_337+68del
NM_020630.6:c.337+58_337+68del NP_065681.1:n.337+58_337+68del