Canonical Allele Identifier: CA1575314022

Gene: COMMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.116261351C= , CM000667.2:g.116261351C=	GRCh38
NC_000005.9:g.115597048C= , CM000667.1:g.115597048C=	GRCh37
NC_000005.8:g.115624947C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274458.9:c.511-30166C= MANE Select	ENSP00000274458.4:n.511-30166C=
ENST00000274458.8:c.511-30166C=	ENSP00000274458.4:n.511-30166C=
ENST00000506589.1:c.268-30166C=	ENSP00000424611.1:n.268-30166C=
ENST00000507356.5:c.*86-30166C=	ENSP00000422448.1:n.*86-30166C=
ENST00000515539.5:c.469-30166C=	ENSP00000427319.1:n.469-30166C=
ENST00000632434.1:c.469-30166C=	ENSP00000488332.1:n.469-30166C=
NM_001308080.1:c.469-30166C=	NP_001295009.1:n.469-30166C=
NM_016144.2:c.511-30166C=	NP_057228.1:n.511-30166C=
NM_016144.3:c.511-30166C=	NP_057228.1:n.511-30166C=
XR_948268.1:n.564-30166C=
XR_948269.1:n.564-30166C=
XR_948270.1:n.564-30166C=
XR_948271.1:n.564-30166C=
XM_017009553.1:c.469-30166C=	XP_016865042.1:n.469-30166C=
XR_001742095.2:n.564-30166C=
XR_001742096.2:n.564-30166C=
XR_001742097.1:n.564-30166C=
XR_001742098.1:n.564-30166C=
XR_001742099.2:n.564-30166C=
XR_001742100.1:n.564-30166C=
XR_001742101.1:n.564-30166C=
XR_002956162.1:n.564-30166C=
XR_948270.2:n.564-30166C=
NM_016144.4:c.511-30166C= MANE Select	NP_057228.1:n.511-30166C=
NM_001308080.2:c.469-30166C=	NP_001295009.1:n.469-30166C=