Canonical Allele Identifier: CA665316795

Gene: RET

Linked Data

• dbSNP Id: rs1445813942
• gnomAD v3: 10-43130188-GTTACTAAGTATTAAGTA-G
• gnomAD v4: 10-43130188-GTTACTAAGTATTAAGTA-G
• MyVariant Identifiers: chr10:g.43625637_43625653del (hg19) ; chr10:g.43130189_43130205del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43130194_43130210del , CM000672.2:g.43130194_43130210del	GRCh38
NC_000010.10:g.43625642_43625658del , CM000672.1:g.43625642_43625658del	GRCh37
NC_000010.9:g.42945648_42945664del	NCBI36
NG_007489.1:g.58126_58142del , LRG_518:g.58126_58142del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615310.5:c.*3440_*3456del	ENSP00000480088.2:n.*3440_*3456del
ENST00000683007.1:n.6233_6249del
ENST00000355710.8:c.*1925_*1941del MANE Select	ENSP00000347942.3:n.*1925_*1941del
ENST00000355710.7:c.*1925_*1941del	ENSP00000347942.3:n.*1925_*1941del
ENST00000615310.4:c.*2619_*2635del	ENSP00000480088.1:n.*2619_*2635del
NM_020975.4:c.*1925_*1941del , LRG_518t1:c.*1925_*1941del	NP_066124.1:n.*1925_*1941del
XM_011540027.1:c.*693_*709del	XP_011538329.1:n.*693_*709del
NM_020975.5:c.*1925_*1941del	NP_066124.1:n.*1925_*1941del
NM_020975.6:c.*1925_*1941del MANE Select	NP_066124.1:n.*1925_*1941del