Canonical Allele Identifier: CA2830536741

Gene: COMMD8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47460455A>T , CM000666.2:g.47460455A>T	GRCh38
NC_000004.11:g.47462472A>T , CM000666.1:g.47462472A>T	GRCh37
NC_000004.10:g.47157229A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381571.6:c.67-156T>A MANE Select	ENSP00000370984.4:n.67-156T>A
ENST00000381571.5:c.67-156T>A	ENSP00000370984.4:n.67-156T>A
ENST00000509220.1:n.81-156T>A
NM_017845.3:c.67-156T>A	NP_060315.1:n.67-156T>A
XM_006714019.1:c.67-156T>A	XP_006714082.1:n.67-156T>A
NM_001329668.1:c.67-156T>A	NP_001316597.1:n.67-156T>A
NM_017845.4:c.67-156T>A	NP_060315.1:n.67-156T>A
XM_017008330.1:c.67-156T>A	XP_016863819.1:n.67-156T>A
NM_017845.5:c.67-156T>A MANE Select	NP_060315.1:n.67-156T>A
NM_001329668.2:c.67-156T>A	NP_001316597.1:n.67-156T>A