Canonical Allele Identifier: CA2248956602

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14069515_14069516delinsAG , CM000679.2:g.14069515_14069516delinsAG	GRCh38
NC_000017.10:g.13972832_13972833delinsAG , CM000679.1:g.13972832_13972833delinsAG	GRCh37
NC_000017.9:g.13913557_13913558delinsAG	NCBI36
NG_008034.1:g.5114_5115delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.-91_-90delinsAG MANE Select	ENSP00000261643.3:n.-91_-90delinsAG
ENST00000664217.1:c.-91_-90delinsAG	ENSP00000499396.1:n.-91_-90delinsAG
ENST00000670279.1:c.-91_-90delinsAG	ENSP00000499450.1:n.-91_-90delinsAG
ENST00000429152.6:c.-91_-90delinsAG	ENSP00000397750.2:n.-91_-90delinsAG
NM_001303.3:c.-91_-90delinsAG	NP_001294.2:n.-91_-90delinsAG
XM_005256458.1:c.-91_-90delinsAG	XP_005256515.1:n.-91_-90delinsAG
XM_011523657.1:c.-91_-90delinsAG	XP_011521959.1:n.-91_-90delinsAG
XM_011523658.1:c.-542_-541delinsAG	XP_011521960.1:n.-542_-541delinsAG
XR_933974.1:n.13_14delinsAG
XR_933975.1:n.13_14delinsAG
NM_001303.4:c.-91_-90delinsAG MANE Select	NP_001294.2:n.-91_-90delinsAG