Canonical Allele Identifier: CA927692923

Gene: RET

Linked Data

• gnomAD v3: 10-43100748-C-CCCCTGCCCCCCCCCCCCCCCTCCTCCAG
• gnomAD v4: 10-43100748-C-CCCCTGCCCCCCCCCCCCCCCTCCTCCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100750_43100751insCTGCCCCCCCCCCCCCCCTCCTCCAGCC , CM000672.2:g.43100750_43100751insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	GRCh38
NC_000010.10:g.43596198_43596199insCTGCCCCCCCCCCCCCCCTCCTCCAGCC , CM000672.1:g.43596198_43596199insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	GRCh37
NC_000010.9:g.42916204_42916205insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	NCBI36
NG_007489.1:g.28682_28683insCTGCCCCCCCCCCCCCCCTCCTCCAGCC , LRG_518:g.28682_28683insCTGCCCCCCCCCCCCCCCTCCTCCAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000480088.2:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
ENST00000683278.1:c.239+28_239+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
ENST00000684216.1:c.239+28_239+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
ENST00000340058.6:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000344798.4:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
ENST00000355710.8:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC MANE Select	ENSP00000347942.3:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
ENST00000638465.1:c.239+28_239+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
ENST00000640619.1:c.239+28_239+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
ENST00000671844.1:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000500541.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
ENST00000672389.1:c.74-10457_74-10456insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000500252.1:n.74-10457_74-10456insCTGCCCCCCCCCCCCCCCTCC...
ENST00000340058.5:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000344798.4:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
ENST00000355710.7:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000347942.3:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
ENST00000498820.5:c.74-11349_74-11348insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000419080.1:n.74-11349_74-11348insCTGCCCCCCCCCCCCCCCTCC...
ENST00000615310.4:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	ENSP00000480088.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCA...
NM_020630.4:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC , LRG_518t2:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	NP_065681.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
NM_020975.4:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC , LRG_518t1:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	NP_066124.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
XM_011540027.1:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	XP_011538329.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC...
NM_020630.5:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	NP_065681.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
NM_020975.5:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	NP_066124.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
NM_020975.6:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC MANE Select	NP_066124.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC
NM_020630.6:c.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC	NP_065681.1:n.337+28_337+29insCTGCCCCCCCCCCCCCCCTCCTCCAGCC