Canonical Allele Identifier: CA398248707

Gene: COX10

Linked Data

• dbSNP Id: rs1170493773
• MyVariant Identifiers: chr17:g.14005456C>T (hg19) ; chr17:g.14102139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102139C>T , CM000679.2:g.14102139C>T	GRCh38
NC_000017.10:g.14005456C>T , CM000679.1:g.14005456C>T	GRCh37
NC_000017.9:g.13946181C>T	NCBI36
NG_008034.1:g.37738C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.521C>T MANE Select	ENSP00000261643.3:p.Ala174Val
ENST00000664217.1:c.521C>T	ENSP00000499396.1:p.Ala174Val
ENST00000670279.1:c.521C>T	ENSP00000499450.1:p.Ala174Val
ENST00000261643.7:c.521C>T	ENSP00000261643.3:p.Ala174Val
ENST00000580561.1:c.*10C>T	ENSP00000462190.1:n.*10C>T
ENST00000581931.5:c.499+25083C>T	ENSP00000462512.1:n.499+25083C>T
NM_001303.3:c.521C>T	NP_001294.2:p.Ala174Val
XM_005256458.1:c.521C>T	XP_005256515.1:p.Ala174Val
XM_011523657.1:c.521C>T	XP_011521959.1:p.Ala174Val
XM_011523658.1:c.48+25083C>T	XP_011521960.1:n.48+25083C>T
XR_933974.1:n.624C>T
XR_933975.1:n.624C>T
NM_001303.4:c.521C>T MANE Select	NP_001294.2:p.Ala174Val