Canonical Allele Identifier: CA2636208022

Gene: COX10

Linked Data

• gnomAD v4: 17-14102330-C-CATA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102331_14102333dup , CM000679.2:g.14102331_14102333dup	GRCh38
NC_000017.10:g.14005648_14005650dup , CM000679.1:g.14005648_14005650dup	GRCh37
NC_000017.9:g.13946373_13946375dup	NCBI36
NG_008034.1:g.37930_37932dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.624+89_624+91dup MANE Select	ENSP00000261643.3:n.624+89_624+91dup
ENST00000664217.1:c.624+89_624+91dup	ENSP00000499396.1:n.624+89_624+91dup
ENST00000670279.1:c.624+89_624+91dup	ENSP00000499450.1:n.624+89_624+91dup
ENST00000261643.7:c.624+89_624+91dup	ENSP00000261643.3:n.624+89_624+91dup
ENST00000580561.1:c.*113+89_*113+91dup	ENSP00000462190.1:n.*113+89_*113+91dup
ENST00000581931.5:c.499+25275_499+25277dup	ENSP00000462512.1:n.499+25275_499+25277dup
NM_001303.3:c.624+89_624+91dup	NP_001294.2:n.624+89_624+91dup
XM_005256458.1:c.624+89_624+91dup	XP_005256515.1:n.624+89_624+91dup
XM_011523657.1:c.624+89_624+91dup	XP_011521959.1:n.624+89_624+91dup
XM_011523658.1:c.48+25275_48+25277dup	XP_011521960.1:n.48+25275_48+25277dup
XR_933974.1:n.727+89_727+91dup
XR_933975.1:n.727+89_727+91dup
NM_001303.4:c.624+89_624+91dup MANE Select	NP_001294.2:n.624+89_624+91dup