Canonical Allele Identifier: CA3377496

Gene: COMMD10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.116291568T>C , CM000667.2:g.116291568T>C	GRCh38
NC_000005.9:g.115627265T>C , CM000667.1:g.115627265T>C	GRCh37
NC_000005.8:g.115655164T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_016144.4:c.562T>C MANE Select	NP_057228.1:p.Tyr188His
ENST00000274458.9:c.562T>C MANE Select	ENSP00000274458.4:p.Tyr188His
NM_001308080.1:c.520T>C	NP_001295009.1:p.Tyr174His
NM_001308080.2:c.520T>C	NP_001295009.1:p.Tyr174His
NM_016144.2:c.562T>C	NP_057228.1:p.Tyr188His
NM_016144.3:c.562T>C	NP_057228.1:p.Tyr188His
ENST00000274458.8:c.562T>C	ENSP00000274458.4:p.Tyr188His
ENST00000506589.1:c.319T>C	ENSP00000424611.1:p.Tyr107His
ENST00000507356.5:c.*137T>C	ENSP00000422448.1:n.*137T>C
ENST00000508250.5:n.30T>C
ENST00000515539.5:c.520T>C	ENSP00000427319.1:p.Tyr174His
ENST00000632434.1:c.520T>C	ENSP00000488332.1:p.Tyr174His
XM_017009553.1:c.520T>C	XP_016865042.1:p.Tyr174His
XR_001742095.2:n.615T>C
XR_001742096.2:n.615T>C
XR_001742097.1:n.615T>C
XR_001742098.1:n.615T>C
XR_001742099.2:n.615T>C
XR_001742100.1:n.615T>C
XR_001742101.1:n.615T>C
XR_002956162.1:n.615T>C
XR_948268.1:n.615T>C
XR_948269.1:n.615T>C
XR_948270.1:n.615T>C
XR_948270.2:n.615T>C
XR_948271.1:n.615T>C