Canonical Allele Identifier: CA2787756026

Gene: RET

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100741_43100742insCCCCCCCCCCCGGCCCCCCCCCC , CM000672.2:g.43100741_43100742insCCCCCCCCCCCGGCCCCCCCCCC	GRCh38
NC_000010.10:g.43596189_43596190insCCCCCCCCCCCGGCCCCCCCCCC , CM000672.1:g.43596189_43596190insCCCCCCCCCCCGGCCCCCCCCCC	GRCh37
NC_000010.9:g.42916195_42916196insCCCCCCCCCCCGGCCCCCCCCCC	NCBI36
NG_007489.1:g.28673_28674insCCCCCCCCCCCGGCCCCCCCCCC , LRG_518:g.28673_28674insCCCCCCCCCCCGGCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000480088.2:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000683278.1:c.239+19_239+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000684216.1:c.239+19_239+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000340058.6:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000344798.4:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000355710.8:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC MANE Select	ENSP00000347942.3:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000638465.1:c.239+19_239+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000640619.1:c.239+19_239+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000671844.1:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000500541.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000672389.1:c.74-10466_74-10465insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000500252.1:n.74-10466_74-10465insCCCCCCCCCCCGGCCCCCCCC...
ENST00000340058.5:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000344798.4:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000355710.7:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000347942.3:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
ENST00000498820.5:c.74-11358_74-11357insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000419080.1:n.74-11358_74-11357insCCCCCCCCCCCGGCCCCCCCC...
ENST00000615310.4:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	ENSP00000480088.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
NM_020630.4:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC , LRG_518t2:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	NP_065681.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
NM_020975.4:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC , LRG_518t1:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	NP_066124.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
XM_011540027.1:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	XP_011538329.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
NM_020630.5:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	NP_065681.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
NM_020975.5:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	NP_066124.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
NM_020975.6:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC MANE Select	NP_066124.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC
NM_020630.6:c.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC	NP_065681.1:n.337+19_337+20insCCCCCCCCCCCGGCCCCCCCCCC