Canonical Allele Identifier: CA398248661

Gene: COX10

Linked Data

• MyVariant Identifiers: chr17:g.14005433A>T (hg19) ; chr17:g.14102116A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14102116A>T , CM000679.2:g.14102116A>T	GRCh38
NC_000017.10:g.14005433A>T , CM000679.1:g.14005433A>T	GRCh37
NC_000017.9:g.13946158A>T	NCBI36
NG_008034.1:g.37715A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261643.8:c.500-2A>T MANE Select	ENSP00000261643.3:n.500-2A>T
ENST00000664217.1:c.500-2A>T	ENSP00000499396.1:n.500-2A>T
ENST00000670279.1:c.500-2A>T	ENSP00000499450.1:n.500-2A>T
ENST00000261643.7:c.500-2A>T	ENSP00000261643.3:n.500-2A>T
ENST00000580561.1:c.178-2A>T	ENSP00000462190.1:n.178-2A>T
ENST00000581931.5:c.499+25060A>T	ENSP00000462512.1:n.499+25060A>T
NM_001303.3:c.500-2A>T	NP_001294.2:n.500-2A>T
XM_005256458.1:c.500-2A>T	XP_005256515.1:n.500-2A>T
XM_011523657.1:c.500-2A>T	XP_011521959.1:n.500-2A>T
XM_011523658.1:c.48+25060A>T	XP_011521960.1:n.48+25060A>T
XR_933974.1:n.603-2A>T
XR_933975.1:n.603-2A>T
NM_001303.4:c.500-2A>T MANE Select	NP_001294.2:n.500-2A>T