Canonical Allele Identifier: CA1455346859
Gene: COMMD8 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000381571.6:c.67-130T= MANE Select ENSP00000370984.4:n.67-130T=
ENST00000381571.5:c.67-130T= ENSP00000370984.4:n.67-130T=
ENST00000509220.1:n.81-130T=
NM_017845.3:c.67-130T= NP_060315.1:n.67-130T=
XM_006714019.1:c.67-130T= XP_006714082.1:n.67-130T=
NM_001329668.1:c.67-130T= NP_001316597.1:n.67-130T=
NM_017845.4:c.67-130T= NP_060315.1:n.67-130T=
XM_017008330.1:c.67-130T= XP_016863819.1:n.67-130T=
NM_017845.5:c.67-130T= MANE Select NP_060315.1:n.67-130T=
NM_001329668.2:c.67-130T= NP_001316597.1:n.67-130T=
Search 100 bp 5'
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