Canonical Allele Identifier: CA2636207221

Gene: COX10

Linked Data

• gnomAD v4: 17-14069522-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14069526del , CM000679.2:g.14069526del	GRCh38
NC_000017.10:g.13972843del , CM000679.1:g.13972843del	GRCh37
NC_000017.9:g.13913568del	NCBI36
NG_008034.1:g.5125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.-80del MANE Select	ENSP00000261643.3:n.-80del
ENST00000664217.1:c.-80del	ENSP00000499396.1:n.-80del
ENST00000670279.1:c.-80del	ENSP00000499450.1:n.-80del
ENST00000429152.6:c.-80del	ENSP00000397750.2:n.-80del
NM_001303.3:c.-80del	NP_001294.2:n.-80del
XM_005256458.1:c.-80del	XP_005256515.1:n.-80del
XM_011523657.1:c.-80del	XP_011521959.1:n.-80del
XM_011523658.1:c.-531del	XP_011521960.1:n.-531del
XR_933974.1:n.24del
XR_933975.1:n.24del
NM_001303.4:c.-80del MANE Select	NP_001294.2:n.-80del