Canonical Allele Identifier: CA2248939352

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102019A= , CM000679.2:g.14102019A=	GRCh38
NC_000017.10:g.14005336A= , CM000679.1:g.14005336A=	GRCh37
NC_000017.9:g.13946061A=	NCBI36
NG_008034.1:g.37618A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.500-99A= MANE Select	ENSP00000261643.3:n.500-99A=
ENST00000664217.1:c.500-99A=	ENSP00000499396.1:n.500-99A=
ENST00000670279.1:c.500-99A=	ENSP00000499450.1:n.500-99A=
ENST00000261643.7:c.500-99A=	ENSP00000261643.3:n.500-99A=
ENST00000580561.1:c.178-99A=	ENSP00000462190.1:n.178-99A=
ENST00000581931.5:c.499+24963A=	ENSP00000462512.1:n.499+24963A=
NM_001303.3:c.500-99A=	NP_001294.2:n.500-99A=
XM_005256458.1:c.500-99A=	XP_005256515.1:n.500-99A=
XM_011523657.1:c.500-99A=	XP_011521959.1:n.500-99A=
XM_011523658.1:c.48+24963A=	XP_011521960.1:n.48+24963A=
XR_933974.1:n.603-99A=
XR_933975.1:n.603-99A=
NM_001303.4:c.500-99A= MANE Select	NP_001294.2:n.500-99A=