Canonical Allele Identifier: CA2636207951

Gene: COX10

Linked Data

• gnomAD v4: 17-14102040-C-CTTGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102043_14102047dup , CM000679.2:g.14102043_14102047dup	GRCh38
NC_000017.10:g.14005360_14005364dup , CM000679.1:g.14005360_14005364dup	GRCh37
NC_000017.9:g.13946085_13946089dup	NCBI36
NG_008034.1:g.37642_37646dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.500-75_500-71dup MANE Select	ENSP00000261643.3:n.500-75_500-71dup
ENST00000664217.1:c.500-75_500-71dup	ENSP00000499396.1:n.500-75_500-71dup
ENST00000670279.1:c.500-75_500-71dup	ENSP00000499450.1:n.500-75_500-71dup
ENST00000261643.7:c.500-75_500-71dup	ENSP00000261643.3:n.500-75_500-71dup
ENST00000580561.1:c.178-75_178-71dup	ENSP00000462190.1:n.178-75_178-71dup
ENST00000581931.5:c.499+24987_499+24991dup	ENSP00000462512.1:n.499+24987_499+24991dup
NM_001303.3:c.500-75_500-71dup	NP_001294.2:n.500-75_500-71dup
XM_005256458.1:c.500-75_500-71dup	XP_005256515.1:n.500-75_500-71dup
XM_011523657.1:c.500-75_500-71dup	XP_011521959.1:n.500-75_500-71dup
XM_011523658.1:c.48+24987_48+24991dup	XP_011521960.1:n.48+24987_48+24991dup
XR_933974.1:n.603-75_603-71dup
XR_933975.1:n.603-75_603-71dup
NM_001303.4:c.500-75_500-71dup MANE Select	NP_001294.2:n.500-75_500-71dup