Canonical Allele Identifier: CA1455346835

Gene: COMMD8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.47460372_47460376delinsCAAAT , CM000666.2:g.47460372_47460376delinsCAAAT	GRCh38
NC_000004.11:g.47462389_47462393delinsCAAAT , CM000666.1:g.47462389_47462393delinsCAAAT	GRCh37
NC_000004.10:g.47157146_47157150delinsCAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381571.6:c.67-77_67-73delinsATTTG MANE Select	ENSP00000370984.4:n.67-77_67-73delinsATTTG
ENST00000381571.5:c.67-77_67-73delinsATTTG	ENSP00000370984.4:n.67-77_67-73delinsATTTG
ENST00000509220.1:n.81-77_81-73delinsATTTG
NM_017845.3:c.67-77_67-73delinsATTTG	NP_060315.1:n.67-77_67-73delinsATTTG
XM_006714019.1:c.67-77_67-73delinsATTTG	XP_006714082.1:n.67-77_67-73delinsATTTG
NM_001329668.1:c.67-77_67-73delinsATTTG	NP_001316597.1:n.67-77_67-73delinsATTTG
NM_017845.4:c.67-77_67-73delinsATTTG	NP_060315.1:n.67-77_67-73delinsATTTG
XM_017008330.1:c.67-77_67-73delinsATTTG	XP_016863819.1:n.67-77_67-73delinsATTTG
NM_017845.5:c.67-77_67-73delinsATTTG MANE Select	NP_060315.1:n.67-77_67-73delinsATTTG
NM_001329668.2:c.67-77_67-73delinsATTTG	NP_001316597.1:n.67-77_67-73delinsATTTG