Canonical Allele Identifier: CA2733003847

Gene: COX10

Linked Data

• dbSNP Id: rs2142200091

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102040_14102041insAA , CM000679.2:g.14102040_14102041insAA	GRCh38
NC_000017.10:g.14005357_14005358insAA , CM000679.1:g.14005357_14005358insAA	GRCh37
NC_000017.9:g.13946082_13946083insAA	NCBI36
NG_008034.1:g.37639_37640insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.500-78_500-77insAA MANE Select	ENSP00000261643.3:n.500-78_500-77insAA
ENST00000664217.1:c.500-78_500-77insAA	ENSP00000499396.1:n.500-78_500-77insAA
ENST00000670279.1:c.500-78_500-77insAA	ENSP00000499450.1:n.500-78_500-77insAA
ENST00000261643.7:c.500-78_500-77insAA	ENSP00000261643.3:n.500-78_500-77insAA
ENST00000580561.1:c.178-78_178-77insAA	ENSP00000462190.1:n.178-78_178-77insAA
ENST00000581931.5:c.499+24984_499+24985insAA	ENSP00000462512.1:n.499+24984_499+24985insAA
NM_001303.3:c.500-78_500-77insAA	NP_001294.2:n.500-78_500-77insAA
XM_005256458.1:c.500-78_500-77insAA	XP_005256515.1:n.500-78_500-77insAA
XM_011523657.1:c.500-78_500-77insAA	XP_011521959.1:n.500-78_500-77insAA
XM_011523658.1:c.48+24984_48+24985insAA	XP_011521960.1:n.48+24984_48+24985insAA
XR_933974.1:n.603-78_603-77insAA
XR_933975.1:n.603-78_603-77insAA
NM_001303.4:c.500-78_500-77insAA MANE Select	NP_001294.2:n.500-78_500-77insAA