Canonical Allele Identifier: CA1575313970
Gene: COMMD10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.116261267C= , CM000667.2:g.116261267C= GRCh38
NC_000005.9:g.115596964C= , CM000667.1:g.115596964C= GRCh37
NC_000005.8:g.115624863C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274458.9:c.511-30250C= MANE Select ENSP00000274458.4:n.511-30250C=
ENST00000274458.8:c.511-30250C= ENSP00000274458.4:n.511-30250C=
ENST00000506589.1:c.268-30250C= ENSP00000424611.1:n.268-30250C=
ENST00000507356.5:c.*86-30250C= ENSP00000422448.1:n.*86-30250C=
ENST00000515539.5:c.469-30250C= ENSP00000427319.1:n.469-30250C=
ENST00000632434.1:c.469-30250C= ENSP00000488332.1:n.469-30250C=
NM_001308080.1:c.469-30250C= NP_001295009.1:n.469-30250C=
NM_016144.2:c.511-30250C= NP_057228.1:n.511-30250C=
NM_016144.3:c.511-30250C= NP_057228.1:n.511-30250C=
XR_948268.1:n.564-30250C=
XR_948269.1:n.564-30250C=
XR_948270.1:n.564-30250C=
XR_948271.1:n.564-30250C=
XM_017009553.1:c.469-30250C= XP_016865042.1:n.469-30250C=
XR_001742095.2:n.564-30250C=
XR_001742096.2:n.564-30250C=
XR_001742097.1:n.564-30250C=
XR_001742098.1:n.564-30250C=
XR_001742099.2:n.564-30250C=
XR_001742100.1:n.564-30250C=
XR_001742101.1:n.564-30250C=
XR_002956162.1:n.564-30250C=
XR_948270.2:n.564-30250C=
NM_016144.4:c.511-30250C= MANE Select NP_057228.1:n.511-30250C=
NM_001308080.2:c.469-30250C= NP_001295009.1:n.469-30250C=