Canonical Allele Identifier: CA726258899

Gene: COX10

Linked Data

• dbSNP Id: rs1367992585
• MyVariant Identifiers: chr17:g.14111991_14111995del (hg19) ; chr17:g.14208674_14208678del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.14208676_14208680del , CM000679.2:g.14208676_14208680del	GRCh38
NC_000017.10:g.14111993_14111997del , CM000679.1:g.14111993_14111997del	GRCh37
NC_000017.9:g.14052718_14052722del	NCBI36
NG_008034.1:g.144275_144279del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000664217.1:c.*178_*182del	ENSP00000499396.1:n.*178_*182del
ENST00000670279.1:c.929-833_929-829del	ENSP00000499450.1:n.929-833_929-829del
XR_933974.1:n.1032-833_1032-829del