Canonical Allele Identifier: CA62839490

Gene: COQ10B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197473812A>G , CM000664.2:g.197473812A>G	GRCh38
NC_000002.11:g.198338536A>G , CM000664.1:g.198338536A>G	GRCh37
NC_000002.10:g.198046781A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025147.5:c.605A>G MANE Select	NP_079423.1:p.Asp202Gly
ENST00000263960.7:c.605A>G MANE Select	ENSP00000263960.2:p.Asp202Gly
NM_001320818.1:c.455A>G	NP_001307747.1:p.Asp152Gly
NM_001320818.2:c.455A>G	NP_001307747.1:p.Asp152Gly
NM_001320819.1:c.521A>G	NP_001307748.1:p.Asp174Gly
NM_001320819.2:c.521A>G	NP_001307748.1:p.Asp174Gly
NM_001320820.1:c.476A>G	NP_001307749.1:p.Asp159Gly
NM_001320820.2:c.476A>G	NP_001307749.1:p.Asp159Gly
NM_025147.3:c.605A>G	NP_079423.1:p.Asp202Gly
NM_025147.4:c.605A>G	NP_079423.1:p.Asp202Gly
ENST00000263960.6:c.605A>G	ENSP00000263960.2:p.Asp202Gly
ENST00000409010.1:c.521A>G	ENSP00000387223.1:p.Asp174Gly
ENST00000409398.5:c.455A>G	ENSP00000386785.1:p.Asp152Gly
XM_006712776.2:c.521A>G	XP_006712839.1:p.Asp174Gly