Canonical Allele Identifier: CA2636207937

Gene: COX10

Linked Data

• gnomAD v4: 17-14102017-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102017C>T , CM000679.2:g.14102017C>T	GRCh38
NC_000017.10:g.14005334C>T , CM000679.1:g.14005334C>T	GRCh37
NC_000017.9:g.13946059C>T	NCBI36
NG_008034.1:g.37616C>T

Transcript Alleles

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