Canonical Allele Identifier: CA2608894406
Gene: RET HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43100745_43100746insCCCCCCCGCCCCCCCCC , CM000672.2:g.43100745_43100746insCCCCCCCGCCCCCCCCC GRCh38
NC_000010.10:g.43596193_43596194insCCCCCCCGCCCCCCCCC , CM000672.1:g.43596193_43596194insCCCCCCCGCCCCCCCCC GRCh37
NC_000010.9:g.42916199_42916200insCCCCCCCGCCCCCCCCC NCBI36
NG_007489.1:g.28677_28678insCCCCCCCGCCCCCCCCC , LRG_518:g.28677_28678insCCCCCCCGCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000615310.5:c.337+23_337+24insCCCCCCCGCCCCCCCCC ENSP00000480088.2:n.337+23_337+24insCCCCCCCGCCCCCCCCC
ENST00000683278.1:c.239+23_239+24insCCCCCCCGCCCCCCCCC
ENST00000684216.1:c.239+23_239+24insCCCCCCCGCCCCCCCCC
ENST00000340058.6:c.337+23_337+24insCCCCCCCGCCCCCCCCC ENSP00000344798.4:n.337+23_337+24insCCCCCCCGCCCCCCCCC
ENST00000355710.8:c.337+23_337+24insCCCCCCCGCCCCCCCCC MANE Select ENSP00000347942.3:n.337+23_337+24insCCCCCCCGCCCCCCCCC
ENST00000638465.1:c.239+23_239+24insCCCCCCCGCCCCCCCCC
ENST00000640619.1:c.239+23_239+24insCCCCCCCGCCCCCCCCC
ENST00000671844.1:c.337+23_337+24insCCCCCCCGCCCCCCCCC ENSP00000500541.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
ENST00000672389.1:c.74-10462_74-10461insCCCCCCCGCCCCCCCCC ENSP00000500252.1:n.74-10462_74-10461insCCCCCCCGCCCCCCCCC
ENST00000340058.5:c.337+23_337+24insCCCCCCCGCCCCCCCCC ENSP00000344798.4:n.337+23_337+24insCCCCCCCGCCCCCCCCC
ENST00000355710.7:c.337+23_337+24insCCCCCCCGCCCCCCCCC ENSP00000347942.3:n.337+23_337+24insCCCCCCCGCCCCCCCCC
ENST00000498820.5:c.74-11354_74-11353insCCCCCCCGCCCCCCCCC ENSP00000419080.1:n.74-11354_74-11353insCCCCCCCGCCCCCCCCC
ENST00000615310.4:c.337+23_337+24insCCCCCCCGCCCCCCCCC ENSP00000480088.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
NM_020630.4:c.337+23_337+24insCCCCCCCGCCCCCCCCC , LRG_518t2:c.337+23_337+24insCCCCCCCGCCCCCCCCC NP_065681.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
NM_020975.4:c.337+23_337+24insCCCCCCCGCCCCCCCCC , LRG_518t1:c.337+23_337+24insCCCCCCCGCCCCCCCCC NP_066124.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
XM_011540027.1:c.337+23_337+24insCCCCCCCGCCCCCCCCC XP_011538329.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
NM_020630.5:c.337+23_337+24insCCCCCCCGCCCCCCCCC NP_065681.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
NM_020975.5:c.337+23_337+24insCCCCCCCGCCCCCCCCC NP_066124.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
NM_020975.6:c.337+23_337+24insCCCCCCCGCCCCCCCCC MANE Select NP_066124.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC
NM_020630.6:c.337+23_337+24insCCCCCCCGCCCCCCCCC NP_065681.1:n.337+23_337+24insCCCCCCCGCCCCCCCCC