Canonical Allele Identifier: CA2248939945

Gene: COX10

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102237_14102240delinsAATC , CM000679.2:g.14102237_14102240delinsAATC	GRCh38
NC_000017.10:g.14005554_14005557delinsAATC , CM000679.1:g.14005554_14005557delinsAATC	GRCh37
NC_000017.9:g.13946279_13946282delinsAATC	NCBI36
NG_008034.1:g.37836_37839delinsAATC

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.619_622delinsAATC MANE Select	ENSP00000261643.3:p.Asn207=
ENST00000664217.1:c.619_622delinsAATC	ENSP00000499396.1:p.Asn207=
ENST00000670279.1:c.619_622delinsAATC	ENSP00000499450.1:p.Asn207=
ENST00000261643.7:c.619_622delinsAATC	ENSP00000261643.3:p.Asn207=
ENST00000580561.1:c.*108_*111delinsAATC	ENSP00000462190.1:n.*108_*111delinsAATC
ENST00000581931.5:c.499+25181_499+25184delinsAATC	ENSP00000462512.1:n.499+25181_499+25184de...
NM_001303.3:c.619_622delinsAATC	NP_001294.2:p.Asn207=
XM_005256458.1:c.619_622delinsAATC	XP_005256515.1:p.Asn207=
XM_011523657.1:c.619_622delinsAATC	XP_011521959.1:p.Asn207=
XM_011523658.1:c.48+25181_48+25184delinsAATC	XP_011521960.1:n.48+25181_48+25184delinsA...
XR_933974.1:n.722_725delinsAATC
XR_933975.1:n.722_725delinsAATC
NM_001303.4:c.619_622delinsAATC MANE Select	NP_001294.2:p.Asn207=