Canonical Allele Identifier: CA2249011199

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208626T= , CM000679.2:g.14208626T=	GRCh38
NC_000017.10:g.14111943T= , CM000679.1:g.14111943T=	GRCh37
NC_000017.9:g.14052668T=	NCBI36
NG_008034.1:g.144225T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1413T= MANE Select	ENSP00000261643.3:n.*1413T=
ENST00000664217.1:c.*128T=	ENSP00000499396.1:n.*128T=
ENST00000670279.1:c.929-883T=	ENSP00000499450.1:n.929-883T=
ENST00000261643.7:c.*1413T=	ENSP00000261643.3:n.*1413T=
NM_001303.3:c.*1413T=	NP_001294.2:n.*1413T=
XM_011523658.1:c.*1413T=	XP_011521960.1:n.*1413T=
XR_933974.1:n.1032-883T=
NM_001303.4:c.*1413T= MANE Select	NP_001294.2:n.*1413T=