Canonical Allele Identifier: CA498438804

Gene: COX10

Linked Data

• MyVariant Identifiers: chr17:g.13980285A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14076968A>T , CM000679.2:g.14076968A>T	GRCh38
NC_000017.10:g.13980285A>T , CM000679.1:g.13980285A>T	GRCh37
NC_000017.9:g.13921010A>T	NCBI36
NG_008034.1:g.12567A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.411A>T MANE Select	ENSP00000261643.3:p.Thr137=
ENST00000664217.1:c.411A>T	ENSP00000499396.1:p.Thr137=
ENST00000670279.1:c.411A>T	ENSP00000499450.1:p.Thr137=
ENST00000261643.7:c.411A>T	ENSP00000261643.3:p.Thr137=
ENST00000429152.6:c.411A>T	ENSP00000397750.2:p.Thr137=
ENST00000580561.1:c.177+2512A>T	ENSP00000462190.1:n.177+2512A>T
ENST00000581931.5:c.411A>T	ENSP00000462512.1:p.Thr137=
NM_001303.3:c.411A>T	NP_001294.2:p.Thr137=
XM_005256458.1:c.411A>T	XP_005256515.1:p.Thr137=
XM_011523657.1:c.411A>T	XP_011521959.1:p.Thr137=
XM_011523658.1:c.-41A>T	XP_011521960.1:n.-41A>T
XR_933974.1:n.514A>T
XR_933975.1:n.514A>T
NM_001303.4:c.411A>T MANE Select	NP_001294.2:p.Thr137=