Canonical Allele Identifier: CA498340744

Gene: COX10

Linked Data

• MyVariant Identifiers: chr17:g.14005460T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102143T>C , CM000679.2:g.14102143T>C	GRCh38
NC_000017.10:g.14005460T>C , CM000679.1:g.14005460T>C	GRCh37
NC_000017.9:g.13946185T>C	NCBI36
NG_008034.1:g.37742T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.525T>C MANE Select	ENSP00000261643.3:p.Ala175=
ENST00000664217.1:c.525T>C	ENSP00000499396.1:p.Ala175=
ENST00000670279.1:c.525T>C	ENSP00000499450.1:p.Ala175=
ENST00000261643.7:c.525T>C	ENSP00000261643.3:p.Ala175=
ENST00000580561.1:c.*14T>C	ENSP00000462190.1:n.*14T>C
ENST00000581931.5:c.499+25087T>C	ENSP00000462512.1:n.499+25087T>C
NM_001303.3:c.525T>C	NP_001294.2:p.Ala175=
XM_005256458.1:c.525T>C	XP_005256515.1:p.Ala175=
XM_011523657.1:c.525T>C	XP_011521959.1:p.Ala175=
XM_011523658.1:c.48+25087T>C	XP_011521960.1:n.48+25087T>C
XR_933974.1:n.628T>C
XR_933975.1:n.628T>C
NM_001303.4:c.525T>C MANE Select	NP_001294.2:p.Ala175=