Canonical Allele Identifier: CA2830543233

Gene: CCDC146

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77293267A>T , CM000669.2:g.77293267A>T	GRCh38
NC_000007.13:g.76922584A>T , CM000669.1:g.76922584A>T	GRCh37
NC_000007.12:g.76760520A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285871.5:c.2664+67A>T MANE Select	ENSP00000285871.4:n.2664+67A>T
ENST00000285871.4:c.2664+67A>T	ENSP00000285871.4:n.2664+67A>T
ENST00000415740.6:n.1851+67A>T
ENST00000461259.5:n.1003+67A>T
ENST00000478101.1:n.473+67A>T
ENST00000488998.1:n.148+67A>T
NM_020879.2:c.2664+67A>T	NP_065930.2:n.2664+67A>T
NM_020879.3:c.2664+67A>T MANE Select	NP_065930.2:n.2664+67A>T