Canonical Allele Identifier: CA11978744

Gene: COMMD10

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.116233060T>C , CM000667.2:g.116233060T>C	GRCh38
NC_000005.9:g.115568757T>C , CM000667.1:g.115568757T>C	GRCh37
NC_000005.8:g.115596656T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274458.9:c.511-58457T>C MANE Select	ENSP00000274458.4:n.511-58457T>C
ENST00000274458.8:c.511-58457T>C	ENSP00000274458.4:n.511-58457T>C
ENST00000506589.1:c.268-58457T>C	ENSP00000424611.1:n.268-58457T>C
ENST00000507356.5:c.*86-58457T>C	ENSP00000422448.1:n.*86-58457T>C
ENST00000515539.5:c.469-58457T>C	ENSP00000427319.1:n.469-58457T>C
ENST00000632434.1:c.469-58457T>C	ENSP00000488332.1:n.469-58457T>C
NM_001308080.1:c.469-58457T>C	NP_001295009.1:n.469-58457T>C
NM_016144.2:c.511-58457T>C	NP_057228.1:n.511-58457T>C
NM_016144.3:c.511-58457T>C	NP_057228.1:n.511-58457T>C
XM_011543460.1:c.511-24022T>C	XP_011541762.1:n.511-24022T>C
XR_948268.1:n.564-58457T>C
XR_948269.1:n.564-58457T>C
XR_948270.1:n.564-58457T>C
XR_948271.1:n.564-58457T>C
XM_011543460.3:c.511-24022T>C	XP_011541762.1:n.511-24022T>C
XM_017009553.1:c.469-58457T>C	XP_016865042.1:n.469-58457T>C
XR_001742095.2:n.564-58457T>C
XR_001742096.2:n.564-58457T>C
XR_001742097.1:n.564-58457T>C
XR_001742098.1:n.564-58457T>C
XR_001742099.2:n.564-58457T>C
XR_001742100.1:n.564-58457T>C
XR_001742101.1:n.564-58457T>C
XR_002956162.1:n.564-58457T>C
XR_948270.2:n.564-58457T>C
NM_016144.4:c.511-58457T>C MANE Select	NP_057228.1:n.511-58457T>C
NM_001308080.2:c.469-58457T>C	NP_001295009.1:n.469-58457T>C