Canonical Allele Identifier: CA2670531444
Gene: COMMD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.47460372_47460375del , CM000666.2:g.47460372_47460375del GRCh38
NC_000004.11:g.47462389_47462392del , CM000666.1:g.47462389_47462392del GRCh37
NC_000004.10:g.47157146_47157149del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381571.6:c.67-70_67-67del MANE Select ENSP00000370984.4:n.67-70_67-67del
ENST00000381571.5:c.67-70_67-67del ENSP00000370984.4:n.67-70_67-67del
ENST00000509220.1:n.81-70_81-67del
NM_017845.3:c.67-70_67-67del NP_060315.1:n.67-70_67-67del
XM_006714019.1:c.67-70_67-67del XP_006714082.1:n.67-70_67-67del
NM_001329668.1:c.67-70_67-67del NP_001316597.1:n.67-70_67-67del
NM_017845.4:c.67-70_67-67del NP_060315.1:n.67-70_67-67del
XM_017008330.1:c.67-70_67-67del XP_016863819.1:n.67-70_67-67del
NM_017845.5:c.67-70_67-67del MANE Select NP_060315.1:n.67-70_67-67del
NM_001329668.2:c.67-70_67-67del NP_001316597.1:n.67-70_67-67del