Canonical Allele Identifier: CA2830543234

Gene: CCDC146

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77293311_77293312insTTCT , CM000669.2:g.77293311_77293312insTTCT	GRCh38
NC_000007.13:g.76922628_76922629insTTCT , CM000669.1:g.76922628_76922629insTTCT	GRCh37
NC_000007.12:g.76760564_76760565insTTCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285871.5:c.2664+111_2664+112insTTCT MANE Select	ENSP00000285871.4:n.2664+111_2664+112insTTCT
ENST00000285871.4:c.2664+111_2664+112insTTCT	ENSP00000285871.4:n.2664+111_2664+112insTTCT
ENST00000415740.6:n.1851+111_1851+112insTTCT
ENST00000461259.5:n.1003+111_1003+112insTTCT
ENST00000478101.1:n.473+111_473+112insTTCT
ENST00000488998.1:n.148+111_148+112insTTCT
NM_020879.2:c.2664+111_2664+112insTTCT	NP_065930.2:n.2664+111_2664+112insTTCT
NM_020879.3:c.2664+111_2664+112insTTCT MANE Select	NP_065930.2:n.2664+111_2664+112insTTCT