Canonical Allele Identifier: CA665362815

Gene: RET

Linked Data

• dbSNP Id: rs1383160997
• gnomAD v3: 10-43077413-CCTTT-C
• gnomAD v4: 10-43077413-CCTTT-C
• MyVariant Identifiers: chr10:g.43572862_43572865del (hg19) ; chr10:g.43077414_43077417del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077416_43077419del , CM000672.2:g.43077416_43077419del	GRCh38
NC_000010.10:g.43572864_43572867del , CM000672.1:g.43572864_43572867del	GRCh37
NC_000010.9:g.42892870_42892873del	NCBI36
NG_007489.1:g.5348_5351del , LRG_518:g.5348_5351del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.73+85_73+88del	ENSP00000480088.2:n.73+85_73+88del
ENST00000340058.6:c.73+85_73+88del	ENSP00000344798.4:n.73+85_73+88del
ENST00000355710.8:c.73+85_73+88del MANE Select	ENSP00000347942.3:n.73+85_73+88del
ENST00000671844.1:c.73+85_73+88del	ENSP00000500541.1:n.73+85_73+88del
ENST00000672389.1:c.73+85_73+88del	ENSP00000500252.1:n.73+85_73+88del
ENST00000340058.5:c.73+85_73+88del	ENSP00000344798.4:n.73+85_73+88del
ENST00000355710.7:c.73+85_73+88del	ENSP00000347942.3:n.73+85_73+88del
ENST00000498820.5:c.73+85_73+88del	ENSP00000419080.1:n.73+85_73+88del
ENST00000615310.4:c.73+85_73+88del	ENSP00000480088.1:n.73+85_73+88del
NM_020630.4:c.73+85_73+88del , LRG_518t2:c.73+85_73+88del	NP_065681.1:n.73+85_73+88del
NM_020975.4:c.73+85_73+88del , LRG_518t1:c.73+85_73+88del	NP_066124.1:n.73+85_73+88del
XM_011540027.1:c.73+85_73+88del	XP_011538329.1:n.73+85_73+88del
NM_020630.5:c.73+85_73+88del	NP_065681.1:n.73+85_73+88del
NM_020975.5:c.73+85_73+88del	NP_066124.1:n.73+85_73+88del
NM_020975.6:c.73+85_73+88del MANE Select	NP_066124.1:n.73+85_73+88del
NM_020630.6:c.73+85_73+88del	NP_065681.1:n.73+85_73+88del