Canonical Allele Identifier: CA398248251

Gene: COX10

Linked Data

• dbSNP Id: rs1398016853
• MyVariant Identifiers: chr17:g.13980211C>A (hg19) ; chr17:g.14076894C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14076894C>A , CM000679.2:g.14076894C>A	GRCh38
NC_000017.10:g.13980211C>A , CM000679.1:g.13980211C>A	GRCh37
NC_000017.9:g.13920936C>A	NCBI36
NG_008034.1:g.12493C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.337C>A MANE Select	ENSP00000261643.3:p.Pro113Thr
ENST00000664217.1:c.337C>A	ENSP00000499396.1:p.Pro113Thr
ENST00000670279.1:c.337C>A	ENSP00000499450.1:p.Pro113Thr
ENST00000261643.7:c.337C>A	ENSP00000261643.3:p.Pro113Thr
ENST00000429152.6:c.337C>A	ENSP00000397750.2:p.Pro113Thr
ENST00000580561.1:c.177+2438C>A	ENSP00000462190.1:n.177+2438C>A
ENST00000581931.5:c.337C>A	ENSP00000462512.1:p.Pro113Thr
NM_001303.3:c.337C>A	NP_001294.2:p.Pro113Thr
XM_005256458.1:c.337C>A	XP_005256515.1:p.Pro113Thr
XM_011523657.1:c.337C>A	XP_011521959.1:p.Pro113Thr
XM_011523658.1:c.-115C>A	XP_011521960.1:n.-115C>A
XR_933974.1:n.440C>A
XR_933975.1:n.440C>A
NM_001303.4:c.337C>A MANE Select	NP_001294.2:p.Pro113Thr