Canonical Allele Identifier: CA1718709275

Gene: CCDC146

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77133468_77133469delinsAT , CM000669.2:g.77133468_77133469delinsAT	GRCh38
NC_000007.13:g.76762785_76762786delinsAT , CM000669.1:g.76762785_76762786delinsAT	GRCh37
NC_000007.12:g.76600721_76600722delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000285871.5:c.-12+10736_-12+10737delinsAT MANE Select	ENSP00000285871.4:n.-12+10736_-12+10737delinsAT
ENST00000285871.4:c.-12+10736_-12+10737delinsAT	ENSP00000285871.4:n.-12+10736_-12+10737delinsAT
ENST00000415750.5:c.-12+11000_-12+11001delinsAT	ENSP00000388649.1:n.-12+11000_-12+11001delinsAT
NM_020879.2:c.-12+10736_-12+10737delinsAT	NP_065930.2:n.-12+10736_-12+10737delinsAT
XR_927691.1:n.48-4743_48-4742delinsAT
NM_020879.3:c.-12+10736_-12+10737delinsAT MANE Select	NP_065930.2:n.-12+10736_-12+10737delinsAT