Canonical Allele Identifier: CA2248939379

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102033_14102050delinsAGGATGGCTTGTTTTTTG , CM000679.2:g.14102033_14102050delinsAGGATGGCTTGTTTTTTG	GRCh38
NC_000017.10:g.14005350_14005367delinsAGGATGGCTTGTTTTTTG , CM000679.1:g.14005350_14005367delinsAGGATGGCTTGTTTTTTG	GRCh37
NC_000017.9:g.13946075_13946092delinsAGGATGGCTTGTTTTTTG	NCBI36
NG_008034.1:g.37632_37649delinsAGGATGGCTTGTTTTTTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG MANE Select	ENSP00000261643.3:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
ENST00000664217.1:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG	ENSP00000499396.1:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
ENST00000670279.1:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG	ENSP00000499450.1:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
ENST00000261643.7:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG	ENSP00000261643.3:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
ENST00000580561.1:c.178-85_178-68delinsAGGATGGCTTGTTTTTTG	ENSP00000462190.1:n.178-85_178-68delinsAGGATGGCTTGTTTTTTG
ENST00000581931.5:c.499+24977_499+24994delinsAGGATGGCTTGTTTTTTG	ENSP00000462512.1:n.499+24977_499+24994delinsAGGATGGCTTGTTTTT...
NM_001303.3:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG	NP_001294.2:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
XM_005256458.1:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG	XP_005256515.1:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
XM_011523657.1:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG	XP_011521959.1:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG
XM_011523658.1:c.48+24977_48+24994delinsAGGATGGCTTGTTTTTTG	XP_011521960.1:n.48+24977_48+24994delinsAGGATGGCTTGTTTTTTG
XR_933974.1:n.603-85_603-68delinsAGGATGGCTTGTTTTTTG
XR_933975.1:n.603-85_603-68delinsAGGATGGCTTGTTTTTTG
NM_001303.4:c.500-85_500-68delinsAGGATGGCTTGTTTTTTG MANE Select	NP_001294.2:n.500-85_500-68delinsAGGATGGCTTGTTTTTTG