Canonical Allele Identifier: CA2248939651

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102127T= , CM000679.2:g.14102127T=	GRCh38
NC_000017.10:g.14005444T= , CM000679.1:g.14005444T=	GRCh37
NC_000017.9:g.13946169T=	NCBI36
NG_008034.1:g.37726T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.509T= MANE Select	ENSP00000261643.3:p.Val170=
ENST00000664217.1:c.509T=	ENSP00000499396.1:p.Val170=
ENST00000670279.1:c.509T=	ENSP00000499450.1:p.Val170=
ENST00000261643.7:c.509T=	ENSP00000261643.3:p.Val170=
ENST00000580561.1:c.187T=	ENSP00000462190.1:p.Ter63=
ENST00000581931.5:c.499+25071T=	ENSP00000462512.1:n.499+25071T=
NM_001303.3:c.509T=	NP_001294.2:p.Val170=
XM_005256458.1:c.509T=	XP_005256515.1:p.Val170=
XM_011523657.1:c.509T=	XP_011521959.1:p.Val170=
XM_011523658.1:c.48+25071T=	XP_011521960.1:n.48+25071T=
XR_933974.1:n.612T=
XR_933975.1:n.612T=
NM_001303.4:c.509T= MANE Select	NP_001294.2:p.Val170=