Canonical Allele Identifier: CA2248939348

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102017_14102021delinsCAATT , CM000679.2:g.14102017_14102021delinsCAATT	GRCh38
NC_000017.10:g.14005334_14005338delinsCAATT , CM000679.1:g.14005334_14005338delinsCAATT	GRCh37
NC_000017.9:g.13946059_13946063delinsCAATT	NCBI36
NG_008034.1:g.37616_37620delinsCAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.500-101_500-97delinsCAATT MANE Select	ENSP00000261643.3:n.500-101_500-97delinsCAATT
ENST00000664217.1:c.500-101_500-97delinsCAATT	ENSP00000499396.1:n.500-101_500-97delinsCAATT
ENST00000670279.1:c.500-101_500-97delinsCAATT	ENSP00000499450.1:n.500-101_500-97delinsCAATT
ENST00000261643.7:c.500-101_500-97delinsCAATT	ENSP00000261643.3:n.500-101_500-97delinsCAATT
ENST00000580561.1:c.178-101_178-97delinsCAATT	ENSP00000462190.1:n.178-101_178-97delinsCAATT
ENST00000581931.5:c.499+24961_499+24965delinsCAATT	ENSP00000462512.1:n.499+24961_499+24965delinsCAATT
NM_001303.3:c.500-101_500-97delinsCAATT	NP_001294.2:n.500-101_500-97delinsCAATT
XM_005256458.1:c.500-101_500-97delinsCAATT	XP_005256515.1:n.500-101_500-97delinsCAATT
XM_011523657.1:c.500-101_500-97delinsCAATT	XP_011521959.1:n.500-101_500-97delinsCAATT
XM_011523658.1:c.48+24961_48+24965delinsCAATT	XP_011521960.1:n.48+24961_48+24965delinsCAATT
XR_933974.1:n.603-101_603-97delinsCAATT
XR_933975.1:n.603-101_603-97delinsCAATT
NM_001303.4:c.500-101_500-97delinsCAATT MANE Select	NP_001294.2:n.500-101_500-97delinsCAATT