Canonical Allele Identifier: CA1718709291

Gene: CCDC146

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77133513A= , CM000669.2:g.77133513A=	GRCh38
NC_000007.13:g.76762830A= , CM000669.1:g.76762830A=	GRCh37
NC_000007.12:g.76600766A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285871.5:c.-12+10781A= MANE Select	ENSP00000285871.4:n.-12+10781A=
ENST00000285871.4:c.-12+10781A=	ENSP00000285871.4:n.-12+10781A=
ENST00000415750.5:c.-12+11045A=	ENSP00000388649.1:n.-12+11045A=
NM_020879.2:c.-12+10781A=	NP_065930.2:n.-12+10781A=
XR_927691.1:n.48-4787T=
NM_020879.3:c.-12+10781A= MANE Select	NP_065930.2:n.-12+10781A=