Canonical Allele Identifier: CA2248956729

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14069554G= , CM000679.2:g.14069554G=	GRCh38
NC_000017.10:g.13972871G= , CM000679.1:g.13972871G=	GRCh37
NC_000017.9:g.13913596G=	NCBI36
NG_008034.1:g.5153G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.-52G= MANE Select	ENSP00000261643.3:n.-52G=
ENST00000664217.1:c.-52G=	ENSP00000499396.1:n.-52G=
ENST00000670279.1:c.-52G=	ENSP00000499450.1:n.-52G=
ENST00000261643.7:c.-52G=	ENSP00000261643.3:n.-52G=
ENST00000429152.6:c.-52G=	ENSP00000397750.2:n.-52G=
NM_001303.3:c.-52G=	NP_001294.2:n.-52G=
XM_005256458.1:c.-52G=	XP_005256515.1:n.-52G=
XM_011523657.1:c.-52G=	XP_011521959.1:n.-52G=
XM_011523658.1:c.-503G=	XP_011521960.1:n.-503G=
XR_933974.1:n.52G=
XR_933975.1:n.52G=
NM_001303.4:c.-52G= MANE Select	NP_001294.2:n.-52G=