Canonical Allele Identifier: CA2248940463

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14159926C= , CM000679.2:g.14159926C=	GRCh38
NC_000017.10:g.14063243C= , CM000679.1:g.14063243C=	GRCh37
NC_000017.9:g.14003968C=	NCBI36
NG_008034.1:g.95525C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001303.4:c.674C= MANE Select	NP_001294.2:p.Pro225=
ENST00000261643.8:c.674C= MANE Select	ENSP00000261643.3:p.Pro225=
NM_001303.3:c.674C=	NP_001294.2:p.Pro225=
ENST00000261643.7:c.674C=	ENSP00000261643.3:p.Pro225=
ENST00000580561.1:c.*163C=	ENSP00000462190.1:n.*163C=
ENST00000581931.5:c.*42C=	ENSP00000462512.1:n.*42C=
ENST00000664217.1:c.674C=	ENSP00000499396.1:p.Pro225=
ENST00000670279.1:c.674C=	ENSP00000499450.1:p.Pro225=
XM_005256458.1:c.674C=	XP_005256515.1:p.Pro225=
XM_011523657.1:c.674C=	XP_011521959.1:p.Pro225=
XM_011523658.1:c.98C=	XP_011521960.1:p.Pro33=
XR_933974.1:n.777C=
XR_933975.1:n.777C=