Canonical Allele Identifier: CA2830543236

Gene: CCDC146

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77294961T>C , CM000669.2:g.77294961T>C	GRCh38
NC_000007.13:g.76924278T>C , CM000669.1:g.76924278T>C	GRCh37
NC_000007.12:g.76762214T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285871.5:c.*95T>C MANE Select	ENSP00000285871.4:n.*95T>C
ENST00000285871.4:c.*95T>C	ENSP00000285871.4:n.*95T>C
ENST00000415740.6:n.2150T>C
ENST00000461259.5:n.1302T>C
ENST00000488998.1:n.424+23T>C
NM_020879.2:c.*95T>C	NP_065930.2:n.*95T>C
NM_020879.3:c.*95T>C MANE Select	NP_065930.2:n.*95T>C