Canonical Allele Identifier: CA2580081454

Gene: RET

Linked Data

• ClinVar Variation Id: 1756637
• ClinVar RCV Id: RCV002378242
• gnomAD v4: 10-43077251-CACGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077252_43077255del , CM000672.2:g.43077252_43077255del	GRCh38
NC_000010.10:g.43572700_43572703del , CM000672.1:g.43572700_43572703del	GRCh37
NC_000010.9:g.42892706_42892709del	NCBI36
NG_007489.1:g.5184_5187del , LRG_518:g.5184_5187del

Transcript Alleles

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