Canonical Allele Identifier: CA2249011140

Gene: COX10

Linked Data

• dbSNP Id: rs1656306463

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208509C>T , CM000679.2:g.14208509C>T	GRCh38
NC_000017.10:g.14111826C>T , CM000679.1:g.14111826C>T	GRCh37
NC_000017.9:g.14052551C>T	NCBI36
NG_008034.1:g.144108C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1296C>T MANE Select	ENSP00000261643.3:n.*1296C>T
ENST00000664217.1:c.*56-45C>T	ENSP00000499396.1:n.*56-45C>T
ENST00000670279.1:c.929-1000C>T	ENSP00000499450.1:n.929-1000C>T
ENST00000261643.7:c.*1296C>T	ENSP00000261643.3:n.*1296C>T
NM_001303.3:c.*1296C>T	NP_001294.2:n.*1296C>T
XM_011523658.1:c.*1296C>T	XP_011521960.1:n.*1296C>T
XR_933974.1:n.1032-1000C>T
NM_001303.4:c.*1296C>T MANE Select	NP_001294.2:n.*1296C>T