Canonical Allele Identifier: CA2249011184

Gene: COX10

Linked Data

• dbSNP Id: rs1906778981

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208601_14208602insTTT , CM000679.2:g.14208601_14208602insTTT	GRCh38
NC_000017.10:g.14111918_14111919insTTT , CM000679.1:g.14111918_14111919insTTT	GRCh37
NC_000017.9:g.14052643_14052644insTTT	NCBI36
NG_008034.1:g.144200_144201insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261643.8:c.*1388_*1389insTTT MANE Select	ENSP00000261643.3:n.*1388_*1389insTTT
ENST00000664217.1:c.*103_*104insTTT	ENSP00000499396.1:n.*103_*104insTTT
ENST00000670279.1:c.929-908_929-907insTTT	ENSP00000499450.1:n.929-908_929-907insTTT
ENST00000261643.7:c.*1388_*1389insTTT	ENSP00000261643.3:n.*1388_*1389insTTT
NM_001303.3:c.*1388_*1389insTTT	NP_001294.2:n.*1388_*1389insTTT
XM_011523658.1:c.*1388_*1389insTTT	XP_011521960.1:n.*1388_*1389insTTT
XR_933974.1:n.1032-908_1032-907insTTT
NM_001303.4:c.*1388_*1389insTTT MANE Select	NP_001294.2:n.*1388_*1389insTTT