Canonical Allele Identifier: CA665327770

Gene: RET

Linked Data

• dbSNP Id: rs1201381707
• gnomAD v3: 10-43106318-TG-T
• gnomAD v4: 10-43106318-TG-T
• MyVariant Identifiers: chr10:g.43601767del (hg19) ; chr10:g.43106319del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43106324del , CM000672.2:g.43106324del	GRCh38
NC_000010.10:g.43601772del , CM000672.1:g.43601772del	GRCh37
NC_000010.9:g.42921778del	NCBI36
NG_007489.1:g.34256del , LRG_518:g.34256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.867+1131del	ENSP00000480088.2:n.867+1131del
ENST00000683007.1:n.442-52del
ENST00000340058.6:c.868-52del	ENSP00000344798.4:n.868-52del
ENST00000355710.8:c.868-52del MANE Select	ENSP00000347942.3:n.868-52del
ENST00000671844.1:c.625+3695del	ENSP00000500541.1:n.625+3695del
ENST00000672389.1:c.74-4883del	ENSP00000500252.1:n.74-4883del
ENST00000340058.5:c.868-52del	ENSP00000344798.4:n.868-52del
ENST00000355710.7:c.868-52del	ENSP00000347942.3:n.868-52del
ENST00000479913.1:n.463-52del
ENST00000498820.5:c.74-5775del	ENSP00000419080.1:n.74-5775del
ENST00000615310.4:c.868-52del	ENSP00000480088.1:n.868-52del
NM_020630.4:c.868-52del , LRG_518t2:c.868-52del	NP_065681.1:n.868-52del
NM_020975.4:c.868-52del , LRG_518t1:c.868-52del	NP_066124.1:n.868-52del
XM_011540027.1:c.868-52del	XP_011538329.1:n.868-52del
NM_001355216.1:c.106-52del	NP_001342145.1:n.106-52del
NM_020630.5:c.868-52del	NP_065681.1:n.868-52del
NM_020975.5:c.868-52del	NP_066124.1:n.868-52del
NM_020975.6:c.868-52del MANE Select	NP_066124.1:n.868-52del
NM_020630.6:c.868-52del	NP_065681.1:n.868-52del