Canonical Allele Identifier: CA125822737

Gene: COMMD10

Linked Data

• dbSNP Id: rs530574178
• MyVariant Identifiers: chr5:g.115512258A>G (hg19) ; chr5:g.116176561A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.116176561A>G , CM000667.2:g.116176561A>G	GRCh38
NC_000005.9:g.115512258A>G , CM000667.1:g.115512258A>G	GRCh37
NC_000005.8:g.115540157A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000274458.9:c.510+42383A>G MANE Select	ENSP00000274458.4:n.510+42383A>G
ENST00000274458.8:c.510+42383A>G	ENSP00000274458.4:n.510+42383A>G
ENST00000506589.1:c.267+83861A>G	ENSP00000424611.1:n.267+83861A>G
ENST00000507356.5:c.*85+42383A>G	ENSP00000422448.1:n.*85+42383A>G
ENST00000515539.5:c.468+42383A>G	ENSP00000427319.1:n.468+42383A>G
ENST00000632434.1:c.468+42383A>G	ENSP00000488332.1:n.468+42383A>G
NM_001308080.1:c.468+42383A>G	NP_001295009.1:n.468+42383A>G
NM_016144.2:c.510+42383A>G	NP_057228.1:n.510+42383A>G
NM_016144.3:c.510+42383A>G	NP_057228.1:n.510+42383A>G
XM_011543458.1:c.511-9318A>G	XP_011541760.1:n.511-9318A>G
XM_011543460.1:c.510+42383A>G	XP_011541762.1:n.510+42383A>G
XM_011543461.1:c.511-3841A>G	XP_011541763.1:n.511-3841A>G
XR_948268.1:n.563+42383A>G
XR_948269.1:n.563+42383A>G
XR_948270.1:n.563+42383A>G
XR_948271.1:n.563+42383A>G
XR_948272.1:n.1919-9318A>G
NR_146218.1:n.588-9318A>G
NR_146219.1:n.635-9318A>G
NR_146220.1:n.588-3841A>G
XM_011543458.3:c.511-9318A>G	XP_011541760.1:n.511-9318A>G
XM_011543460.3:c.510+42383A>G	XP_011541762.1:n.510+42383A>G
XM_017009553.1:c.468+42383A>G	XP_016865042.1:n.468+42383A>G
XR_001742095.2:n.563+42383A>G
XR_001742096.2:n.563+42383A>G
XR_001742097.1:n.563+42383A>G
XR_001742098.1:n.563+42383A>G
XR_001742099.2:n.563+42383A>G
XR_001742100.1:n.563+42383A>G
XR_001742101.1:n.563+42383A>G
XR_002956162.1:n.563+42383A>G
XR_948270.2:n.563+42383A>G
NM_016144.4:c.510+42383A>G MANE Select	NP_057228.1:n.510+42383A>G
NR_146218.2:n.539-9318A>G
NR_146220.2:n.539-3841A>G
NM_001308080.2:c.468+42383A>G	NP_001295009.1:n.468+42383A>G
NR_146219.2:n.635-9318A>G