Canonical Allele Identifier: CA2636207930

Gene: COX10

Linked Data

• gnomAD v4: 17-14102008-TAATATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102010_14102015del , CM000679.2:g.14102010_14102015del	GRCh38
NC_000017.10:g.14005327_14005332del , CM000679.1:g.14005327_14005332del	GRCh37
NC_000017.9:g.13946052_13946057del	NCBI36
NG_008034.1:g.37609_37614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.500-108_500-103del MANE Select	ENSP00000261643.3:n.500-108_500-103del
ENST00000664217.1:c.500-108_500-103del	ENSP00000499396.1:n.500-108_500-103del
ENST00000670279.1:c.500-108_500-103del	ENSP00000499450.1:n.500-108_500-103del
ENST00000261643.7:c.500-108_500-103del	ENSP00000261643.3:n.500-108_500-103del
ENST00000580561.1:c.178-108_178-103del	ENSP00000462190.1:n.178-108_178-103del
ENST00000581931.5:c.499+24954_499+24959del	ENSP00000462512.1:n.499+24954_499+24959del
NM_001303.3:c.500-108_500-103del	NP_001294.2:n.500-108_500-103del
XM_005256458.1:c.500-108_500-103del	XP_005256515.1:n.500-108_500-103del
XM_011523657.1:c.500-108_500-103del	XP_011521959.1:n.500-108_500-103del
XM_011523658.1:c.48+24954_48+24959del	XP_011521960.1:n.48+24954_48+24959del
XR_933974.1:n.603-108_603-103del
XR_933975.1:n.603-108_603-103del
NM_001303.4:c.500-108_500-103del MANE Select	NP_001294.2:n.500-108_500-103del