Canonical Allele Identifier: CA2610489102

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99713751C>A , CM000672.2:g.99713751C>A GRCh38
NC_000010.10:g.101473508C>A , CM000672.1:g.101473508C>A GRCh37
NC_000010.9:g.101463498C>A NCBI36
NG_008986.1:g.23916G>T , LRG_406:g.23916G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000016171.6:c.*836G>T (COX15) MANE Select ENSP00000016171.6:n.*836G>T
ENST00000649102.1:c.*460+2597G>T ENSP00000497114.1:n.*460+2597G>T
ENST00000016171.5:c.*836G>T (COX15) ENSP00000016171.5:n.*836G>T
ENST00000370483.9:c.1102-272G>T (COX15) ENSP00000359514.5:n.1102-272G>T
ENST00000493385.5:n.117-9167C>A (CUTC)
NM_004376.5:c.1102-272G>T , LRG_406t2:c.1102-272G>T (COX15) NP_004367.2:n.1102-272G>T
NM_078470.4:c.*836G>T , LRG_406t1:c.*836G>T (COX15) NP_510870.1:n.*836G>T
XM_005269539.3:c.1101+2597G>T (COX15) XP_005269596.1:n.1101+2597G>T
XM_006717633.2:c.*1017G>T (COX15) XP_006717696.1:n.*1017G>T
XM_006717634.2:c.*49+2597G>T (COX15) XP_006717697.1:n.*49+2597G>T
XM_011539298.1:c.*50-272G>T (COX15) XP_011537600.1:n.*50-272G>T
NM_001320974.1:c.1101+2597G>T (COX15) NP_001307903.1:n.1101+2597G>T
NM_001320975.1:c.*1017G>T (COX15) NP_001307904.1:n.*1017G>T
NM_001320976.1:c.*836G>T (COX15) NP_001307905.1:n.*836G>T
NM_004376.6:c.1102-272G>T (COX15) NP_004367.2:n.1102-272G>T
NM_078470.5:c.*836G>T (COX15) NP_510870.1:n.*836G>T
XM_006717634.3:c.*49+2597G>T (COX15) XP_006717697.1:n.*49+2597G>T
XM_011539298.2:c.*50-272G>T (COX15) XP_011537600.1:n.*50-272G>T
NM_001320974.2:c.1101+2597G>T (COX15) NP_001307903.1:n.1101+2597G>T
NM_001320975.2:c.*1017G>T (COX15) NP_001307904.1:n.*1017G>T
NM_001320976.2:c.*836G>T (COX15) NP_001307905.1:n.*836G>T
NM_001372024.1:c.*55G>T (COX15) NP_001358953.1:n.*55G>T
NM_001372025.1:c.*836G>T (COX15) NP_001358954.1:n.*836G>T
NM_001372026.1:c.*836G>T (COX15) NP_001358955.1:n.*836G>T
NM_001372027.1:c.*940G>T (COX15) NP_001358956.1:n.*940G>T
NM_001372028.1:c.*263G>T (COX15) NP_001358957.1:n.*263G>T
NM_004376.7:c.1102-272G>T (COX15) NP_004367.2:n.1102-272G>T
NM_078470.6:c.*836G>T (COX15) MANE Select NP_510870.1:n.*836G>T
NR_164009.1:n.1909G>T (COX15)