Canonical Allele Identifier: CA593292842

Gene: RET

Linked Data

• gnomAD v2: 10-43596201-G-GT
• gnomAD v4: 10-43100753-G-GT
• MyVariant Identifiers: chr10:g.43596202_43596226delinsTCCCCACCCCACCCCTTCCTCAAGCC (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43100753_43100754insT , CM000672.2:g.43100753_43100754insT	GRCh38
NC_000010.10:g.43596201_43596202insT , CM000672.1:g.43596201_43596202insT	GRCh37
NC_000010.9:g.42916207_42916208insT	NCBI36
NG_007489.1:g.28685_28686insT , LRG_518:g.28685_28686insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.337+31_337+32insT	ENSP00000480088.2:n.337+31_337+32insT
ENST00000683278.1:c.239+31_239+32insT
ENST00000684216.1:c.239+31_239+32insT
ENST00000340058.6:c.337+31_337+32insT	ENSP00000344798.4:n.337+31_337+32insT
ENST00000355710.8:c.337+31_337+32insT MANE Select	ENSP00000347942.3:n.337+31_337+32insT
ENST00000638465.1:c.239+31_239+32insT
ENST00000640619.1:c.239+31_239+32insT
ENST00000671844.1:c.337+31_337+32insT	ENSP00000500541.1:n.337+31_337+32insT
ENST00000672389.1:c.74-10454_74-10453insT	ENSP00000500252.1:n.74-10454_74-10453insT
ENST00000340058.5:c.337+31_337+32insT	ENSP00000344798.4:n.337+31_337+32insT
ENST00000355710.7:c.337+31_337+32insT	ENSP00000347942.3:n.337+31_337+32insT
ENST00000498820.5:c.74-11346_74-11345insT	ENSP00000419080.1:n.74-11346_74-11345insT
ENST00000615310.4:c.337+31_337+32insT	ENSP00000480088.1:n.337+31_337+32insT
NM_020630.4:c.337+31_337+32insT , LRG_518t2:c.337+31_337+32insT	NP_065681.1:n.337+31_337+32insT
NM_020975.4:c.337+31_337+32insT , LRG_518t1:c.337+31_337+32insT	NP_066124.1:n.337+31_337+32insT
XM_011540027.1:c.337+31_337+32insT	XP_011538329.1:n.337+31_337+32insT
NM_020630.5:c.337+31_337+32insT	NP_065681.1:n.337+31_337+32insT
NM_020975.5:c.337+31_337+32insT	NP_066124.1:n.337+31_337+32insT
NM_020975.6:c.337+31_337+32insT MANE Select	NP_066124.1:n.337+31_337+32insT
NM_020630.6:c.337+31_337+32insT	NP_065681.1:n.337+31_337+32insT