Canonical Allele Identifier: CA398248898

Gene: COX10

Linked Data

• MyVariant Identifiers: chr17:g.14005552T>A (hg19) ; chr17:g.14102235T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102235T>A , CM000679.2:g.14102235T>A	GRCh38
NC_000017.10:g.14005552T>A , CM000679.1:g.14005552T>A	GRCh37
NC_000017.9:g.13946277T>A	NCBI36
NG_008034.1:g.37834T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.617T>A MANE Select	ENSP00000261643.3:p.Ile206Asn
ENST00000664217.1:c.617T>A	ENSP00000499396.1:p.Ile206Asn
ENST00000670279.1:c.617T>A	ENSP00000499450.1:p.Ile206Asn
ENST00000261643.7:c.617T>A	ENSP00000261643.3:p.Ile206Asn
ENST00000580561.1:c.*106T>A	ENSP00000462190.1:n.*106T>A
ENST00000581931.5:c.499+25179T>A	ENSP00000462512.1:n.499+25179T>A
NM_001303.3:c.617T>A	NP_001294.2:p.Ile206Asn
XM_005256458.1:c.617T>A	XP_005256515.1:p.Ile206Asn
XM_011523657.1:c.617T>A	XP_011521959.1:p.Ile206Asn
XM_011523658.1:c.48+25179T>A	XP_011521960.1:n.48+25179T>A
XR_933974.1:n.720T>A
XR_933975.1:n.720T>A
NM_001303.4:c.617T>A MANE Select	NP_001294.2:p.Ile206Asn