Canonical Allele Identifier: CA2608894000

Gene: RET

Linked Data

• gnomAD v4: 10-43077029-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.43077029_43077030insA , CM000672.2:g.43077029_43077030insA	GRCh38
NC_000010.10:g.43572477_43572478insA , CM000672.1:g.43572477_43572478insA	GRCh37
NC_000010.9:g.42892483_42892484insA	NCBI36
NG_007489.1:g.4961_4962insA , LRG_518:g.4961_4962insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355710.7:c.-230_-229insA	ENSP00000347942.3:n.-230_-229insA
XM_011540027.1:c.-230_-229insA	XP_011538329.1:n.-230_-229insA
NM_020630.5:c.-230_-229insA	NP_065681.1:n.-230_-229insA
NM_020975.5:c.-230_-229insA	NP_066124.1:n.-230_-229insA