Canonical Allele Identifier: CA593292830

Gene: RET

Linked Data

• gnomAD v2: 10-43596190-A-ACCCCCCCCCCGCCCCCCC
• gnomAD v3: 10-43100742-A-ACCCCCCCCCCGCCCCCCC
• gnomAD v4: 10-43100742-A-ACCCCCCCCCCGCCCCCCC
• MyVariant Identifiers: chr10:g.43596190_43596191insCCCCCCCCCCGCCCCCCC (hg19) ; chr10:g.43100742_43100743insCCCCCCCCCCGCCCCCCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100745_43100746insCCCCCCCGCCCCCCCCCC , CM000672.2:g.43100745_43100746insCCCCCCCGCCCCCCCCCC	GRCh38
NC_000010.10:g.43596193_43596194insCCCCCCCGCCCCCCCCCC , CM000672.1:g.43596193_43596194insCCCCCCCGCCCCCCCCCC	GRCh37
NC_000010.9:g.42916199_42916200insCCCCCCCGCCCCCCCCCC	NCBI36
NG_007489.1:g.28677_28678insCCCCCCCGCCCCCCCCCC , LRG_518:g.28677_28678insCCCCCCCGCCCCCCCCCC

Transcript Alleles

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