Canonical Allele Identifier: CA398248298

Gene: COX10

Linked Data

• MyVariant Identifiers: chr17:g.13980230T>A (hg19) ; chr17:g.14076913T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14076913T>A , CM000679.2:g.14076913T>A	GRCh38
NC_000017.10:g.13980230T>A , CM000679.1:g.13980230T>A	GRCh37
NC_000017.9:g.13920955T>A	NCBI36
NG_008034.1:g.12512T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.356T>A MANE Select	ENSP00000261643.3:p.Ile119Lys
ENST00000664217.1:c.356T>A	ENSP00000499396.1:p.Ile119Lys
ENST00000670279.1:c.356T>A	ENSP00000499450.1:p.Ile119Lys
ENST00000261643.7:c.356T>A	ENSP00000261643.3:p.Ile119Lys
ENST00000429152.6:c.356T>A	ENSP00000397750.2:p.Ile119Lys
ENST00000580561.1:c.177+2457T>A	ENSP00000462190.1:n.177+2457T>A
ENST00000581931.5:c.356T>A	ENSP00000462512.1:p.Ile119Lys
NM_001303.3:c.356T>A	NP_001294.2:p.Ile119Lys
XM_005256458.1:c.356T>A	XP_005256515.1:p.Ile119Lys
XM_011523657.1:c.356T>A	XP_011521959.1:p.Ile119Lys
XM_011523658.1:c.-96T>A	XP_011521960.1:n.-96T>A
XR_933974.1:n.459T>A
XR_933975.1:n.459T>A
NM_001303.4:c.356T>A MANE Select	NP_001294.2:p.Ile119Lys