Canonical Allele Identifier: CA2830543235

Gene: CCDC146

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.77293312_77293313insACGACTGTTGGGACTGTGTGTG , CM000669.2:g.77293312_77293313insACGACTGTTGGGACTGTGTGTG	GRCh38
NC_000007.13:g.76922629_76922630insACGACTGTTGGGACTGTGTGTG , CM000669.1:g.76922629_76922630insACGACTGTTGGGACTGTGTGTG	GRCh37
NC_000007.12:g.76760565_76760566insACGACTGTTGGGACTGTGTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285871.5:c.2664+112_2664+113insACGACTGTTGGGACTGTGTGTG MANE Select	ENSP00000285871.4:n.2664+112_2664+113insACGACTGTTGGGACTGTGTGT...
ENST00000285871.4:c.2664+112_2664+113insACGACTGTTGGGACTGTGTGTG	ENSP00000285871.4:n.2664+112_2664+113insACGACTGTTGGGACTGTGTGT...
ENST00000415740.6:n.1851+112_1851+113insACGACTGTTGGGACTGTGTGTG
ENST00000461259.5:n.1003+112_1003+113insACGACTGTTGGGACTGTGTGTG
ENST00000478101.1:n.473+112_473+113insACGACTGTTGGGACTGTGTGTG
ENST00000488998.1:n.148+112_148+113insACGACTGTTGGGACTGTGTGTG
NM_020879.2:c.2664+112_2664+113insACGACTGTTGGGACTGTGTGTG	NP_065930.2:n.2664+112_2664+113insACGACTGTTGGGACTGTGTGTG
NM_020879.3:c.2664+112_2664+113insACGACTGTTGGGACTGTGTGTG MANE Select	NP_065930.2:n.2664+112_2664+113insACGACTGTTGGGACTGTGTGTG