Canonical Allele Identifier: CA1931452975

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99714623A= , CM000672.2:g.99714623A= GRCh38
NC_000010.10:g.101474380A= , CM000672.1:g.101474380A= GRCh37
NC_000010.9:g.101464370A= NCBI36
NG_008986.1:g.23044T= , LRG_406:g.23044T=

Transcript Alleles

HGVS Amino-acid change
ENST00000016171.6:c.1197T= (COX15) MANE Select ENSP00000016171.6:p.Leu399=
ENST00000649102.1:c.*460+1725T= ENSP00000497114.1:n.*460+1725T=
ENST00000016171.5:c.1197T= (COX15) ENSP00000016171.5:p.Leu399=
ENST00000370483.9:c.1102-1144T= (COX15) ENSP00000359514.5:n.1102-1144T=
ENST00000493385.5:n.117-8295A= (CUTC)
NM_004376.5:c.1102-1144T= , LRG_406t2:c.1102-1144T= (COX15) NP_004367.2:n.1102-1144T=
NM_078470.4:c.1197T= , LRG_406t1:c.1197T= (COX15) NP_510870.1:p.Leu399=
XM_005269539.3:c.1101+1725T= (COX15) XP_005269596.1:n.1101+1725T=
XM_006717633.2:c.*145T= (COX15) XP_006717696.1:n.*145T=
XM_006717634.2:c.*49+1725T= (COX15) XP_006717697.1:n.*49+1725T=
XM_011539298.1:c.*50-1144T= (COX15) XP_011537600.1:n.*50-1144T=
NM_001320974.1:c.1101+1725T= (COX15) NP_001307903.1:n.1101+1725T=
NM_001320975.1:c.*145T= (COX15) NP_001307904.1:n.*145T=
NM_001320976.1:c.660T= (COX15) NP_001307905.1:p.Leu220=
NM_004376.6:c.1102-1144T= (COX15) NP_004367.2:n.1102-1144T=
NM_078470.5:c.1197T= (COX15) NP_510870.1:p.Leu399=
XM_006717634.3:c.*49+1725T= (COX15) XP_006717697.1:n.*49+1725T=
XM_011539298.2:c.*50-1144T= (COX15) XP_011537600.1:n.*50-1144T=
NM_001320974.2:c.1101+1725T= (COX15) NP_001307903.1:n.1101+1725T=
NM_001320975.2:c.*145T= (COX15) NP_001307904.1:n.*145T=
NM_001320976.2:c.660T= (COX15) NP_001307905.1:p.Leu220=
NM_001372024.1:c.1102-659T= (COX15) NP_001358953.1:n.1102-659T=
NM_001372025.1:c.1215T= (COX15) NP_001358954.1:p.Leu405=
NM_001372026.1:c.1170T= (COX15) NP_001358955.1:p.Leu390=
NM_001372027.1:c.*68T= (COX15) NP_001358956.1:n.*68T=
NM_001372028.1:c.*50-659T= (COX15) NP_001358957.1:n.*50-659T=
NM_004376.7:c.1102-1144T= (COX15) NP_004367.2:n.1102-1144T=
NM_078470.6:c.1197T= (COX15) MANE Select NP_510870.1:p.Leu399=
NR_164009.1:n.1037T= (COX15)