Canonical Allele Identifier: CA2670531477

Gene: COMMD8

Linked Data

• gnomAD v4: 4-47460426-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47460429dup , CM000666.2:g.47460429dup	GRCh38
NC_000004.11:g.47462446dup , CM000666.1:g.47462446dup	GRCh37
NC_000004.10:g.47157203dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381571.6:c.67-128dup MANE Select	ENSP00000370984.4:n.67-128dup
ENST00000381571.5:c.67-128dup	ENSP00000370984.4:n.67-128dup
ENST00000509220.1:n.81-128dup
NM_017845.3:c.67-128dup	NP_060315.1:n.67-128dup
XM_006714019.1:c.67-128dup	XP_006714082.1:n.67-128dup
NM_001329668.1:c.67-128dup	NP_001316597.1:n.67-128dup
NM_017845.4:c.67-128dup	NP_060315.1:n.67-128dup
XM_017008330.1:c.67-128dup	XP_016863819.1:n.67-128dup
NM_017845.5:c.67-128dup MANE Select	NP_060315.1:n.67-128dup
NM_001329668.2:c.67-128dup	NP_001316597.1:n.67-128dup