Canonical Allele Identifier: CA1455346860

Gene: COMMD8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47460430C= , CM000666.2:g.47460430C=	GRCh38
NC_000004.11:g.47462447C= , CM000666.1:g.47462447C=	GRCh37
NC_000004.10:g.47157204C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381571.6:c.67-131G= MANE Select	ENSP00000370984.4:n.67-131G=
ENST00000381571.5:c.67-131G=	ENSP00000370984.4:n.67-131G=
ENST00000509220.1:n.81-131G=
NM_017845.3:c.67-131G=	NP_060315.1:n.67-131G=
XM_006714019.1:c.67-131G=	XP_006714082.1:n.67-131G=
NM_001329668.1:c.67-131G=	NP_001316597.1:n.67-131G=
NM_017845.4:c.67-131G=	NP_060315.1:n.67-131G=
XM_017008330.1:c.67-131G=	XP_016863819.1:n.67-131G=
NM_017845.5:c.67-131G= MANE Select	NP_060315.1:n.67-131G=
NM_001329668.2:c.67-131G=	NP_001316597.1:n.67-131G=