Canonical Allele Identifier: CA2248956795

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14069562A= , CM000679.2:g.14069562A=	GRCh38
NC_000017.10:g.13972879A= , CM000679.1:g.13972879A=	GRCh37
NC_000017.9:g.13913604A=	NCBI36
NG_008034.1:g.5161A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.-44A= MANE Select	ENSP00000261643.3:n.-44A=
ENST00000664217.1:c.-44A=	ENSP00000499396.1:n.-44A=
ENST00000670279.1:c.-44A=	ENSP00000499450.1:n.-44A=
ENST00000261643.7:c.-44A=	ENSP00000261643.3:n.-44A=
ENST00000429152.6:c.-44A=	ENSP00000397750.2:n.-44A=
NM_001303.3:c.-44A=	NP_001294.2:n.-44A=
XM_005256458.1:c.-44A=	XP_005256515.1:n.-44A=
XM_011523657.1:c.-44A=	XP_011521959.1:n.-44A=
XM_011523658.1:c.-495A=	XP_011521960.1:n.-495A=
XR_933974.1:n.60A=
XR_933975.1:n.60A=
NM_001303.4:c.-44A= MANE Select	NP_001294.2:n.-44A=