Canonical Allele Identifier: CA5642275

Gene: COX15 CUTC

Linked Data

• ClinVar Variation Id: 1642107
• ClinVar RCV Id: RCV002143146
• dbSNP Id: rs778221503
• ExAC: 10:101486922 T / C
• gnomAD v2: 10-101486922-T-C
• gnomAD v3: 10-99727165-T-C
• gnomAD v4: 10-99727165-T-C
• MyVariant Identifiers: chr10:g.101486922T>C (hg19) ; chr10:g.99727165T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99727165T>C , CM000672.2:g.99727165T>C	GRCh38
NC_000010.10:g.101486922T>C , CM000672.1:g.101486922T>C	GRCh37
NC_000010.9:g.101476912T>C	NCBI36
NG_008986.1:g.10502A>G , LRG_406:g.10502A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000016171.6:c.396-11A>G (COX15) MANE Select	ENSP00000016171.6:n.396-11A>G
ENST00000649102.1:c.396-94A>G	ENSP00000497114.1:n.396-94A>G
ENST00000016171.5:c.396-11A>G (COX15)	ENSP00000016171.5:n.396-11A>G
ENST00000370483.9:c.396-11A>G (COX15)	ENSP00000359514.5:n.396-11A>G
ENST00000493385.5:n.309+4055T>C (CUTC)
NM_004376.5:c.396-11A>G , LRG_406t2:c.396-11A>G (COX15)	NP_004367.2:n.396-11A>G
NM_078470.4:c.396-11A>G , LRG_406t1:c.396-11A>G (COX15)	NP_510870.1:n.396-11A>G
XM_005269539.3:c.396-11A>G (COX15)	XP_005269596.1:n.396-11A>G
XM_006717633.2:c.396-11A>G (COX15)	XP_006717696.1:n.396-11A>G
XM_006717634.2:c.396-11A>G (COX15)	XP_006717697.1:n.396-11A>G
XM_011539298.1:c.396-11A>G (COX15)	XP_011537600.1:n.396-11A>G
NM_001320974.1:c.396-11A>G (COX15)	NP_001307903.1:n.396-11A>G
NM_001320975.1:c.396-11A>G (COX15)	NP_001307904.1:n.396-11A>G
NM_001320976.1:c.-59-94A>G (COX15)	NP_001307905.1:n.-59-94A>G
NM_004376.6:c.396-11A>G (COX15)	NP_004367.2:n.396-11A>G
NM_078470.5:c.396-11A>G (COX15)	NP_510870.1:n.396-11A>G
XM_006717634.3:c.396-11A>G (COX15)	XP_006717697.1:n.396-11A>G
XM_011539298.2:c.396-11A>G (COX15)	XP_011537600.1:n.396-11A>G
NM_001320974.2:c.396-11A>G (COX15)	NP_001307903.1:n.396-11A>G
NM_001320975.2:c.396-11A>G (COX15)	NP_001307904.1:n.396-11A>G
NM_001320976.2:c.-59-94A>G (COX15)	NP_001307905.1:n.-59-94A>G
NM_001372024.1:c.396-11A>G (COX15)	NP_001358953.1:n.396-11A>G
NM_001372025.1:c.396-11A>G (COX15)	NP_001358954.1:n.396-11A>G
NM_001372026.1:c.396-11A>G (COX15)	NP_001358955.1:n.396-11A>G
NM_001372027.1:c.396-11A>G (COX15)	NP_001358956.1:n.396-11A>G
NM_001372028.1:c.396-11A>G (COX15)	NP_001358957.1:n.396-11A>G
NM_004376.7:c.396-11A>G (COX15)	NP_004367.2:n.396-11A>G
NM_078470.6:c.396-11A>G (COX15) MANE Select	NP_510870.1:n.396-11A>G
NR_164009.1:n.474-94A>G (COX15)