Canonical Allele Identifier: CA2610489774

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99727182_99727183insTGTTTCCTCCTCCTCCTTTTTT , CM000672.2:g.99727182_99727183insTGTTTCCTCCTCCTCCTTTTTT GRCh38
NC_000010.10:g.101486939_101486940insTGTTTCCTCCTCCTCCTTTTTT , CM000672.1:g.101486939_101486940insTGTTTCCTCCTCCTCCTTTTTT GRCh37
NC_000010.9:g.101476929_101476930insTGTTTCCTCCTCCTCCTTTTTT NCBI36
NG_008986.1:g.10484_10485insAAAAAAGGAGGAGGAGGAAACA , LRG_406:g.10484_10485insAAAAAAGGAGGAGGAGGAAACA

Transcript Alleles

HGVS Amino-acid change
ENST00000016171.6:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) MANE Select ENSP00000016171.6:n.396-29_396-28insAAAAA...
ENST00000649102.1:c.396-112_396-111insAAAAAAGGAGGAGGAGGAAACA ENSP00000497114.1:n.396-112_396-111insAAA...
ENST00000016171.5:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) ENSP00000016171.5:n.396-29_396-28insAAAAA...
ENST00000370483.9:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) ENSP00000359514.5:n.396-29_396-28insAAAAA...
ENST00000493385.5:n.309+4072_309+4073insTGTTTCCTCCTCCTCCTTTTTT (CUTC)
NM_004376.5:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA , LRG_406t2:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_004367.2:n.396-29_396-28insAAAAAAGGAGG...
NM_078470.4:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA , LRG_406t1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_510870.1:n.396-29_396-28insAAAAAAGGAGG...
XM_005269539.3:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) XP_005269596.1:n.396-29_396-28insAAAAAAGG...
XM_006717633.2:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) XP_006717696.1:n.396-29_396-28insAAAAAAGG...
XM_006717634.2:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) XP_006717697.1:n.396-29_396-28insAAAAAAGG...
XM_011539298.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) XP_011537600.1:n.396-29_396-28insAAAAAAGG...
NM_001320974.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001307903.1:n.396-29_396-28insAAAAAAGG...
NM_001320975.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001307904.1:n.396-29_396-28insAAAAAAGG...
NM_001320976.1:c.-59-112_-59-111insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001307905.1:n.-59-112_-59-111insAAAAAA...
NM_004376.6:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_004367.2:n.396-29_396-28insAAAAAAGGAGG...
NM_078470.5:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_510870.1:n.396-29_396-28insAAAAAAGGAGG...
XM_006717634.3:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) XP_006717697.1:n.396-29_396-28insAAAAAAGG...
XM_011539298.2:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) XP_011537600.1:n.396-29_396-28insAAAAAAGG...
NM_001320974.2:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001307903.1:n.396-29_396-28insAAAAAAGG...
NM_001320975.2:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001307904.1:n.396-29_396-28insAAAAAAGG...
NM_001320976.2:c.-59-112_-59-111insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001307905.1:n.-59-112_-59-111insAAAAAA...
NM_001372024.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001358953.1:n.396-29_396-28insAAAAAAGG...
NM_001372025.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001358954.1:n.396-29_396-28insAAAAAAGG...
NM_001372026.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001358955.1:n.396-29_396-28insAAAAAAGG...
NM_001372027.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001358956.1:n.396-29_396-28insAAAAAAGG...
NM_001372028.1:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_001358957.1:n.396-29_396-28insAAAAAAGG...
NM_004376.7:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) NP_004367.2:n.396-29_396-28insAAAAAAGGAGG...
NM_078470.6:c.396-29_396-28insAAAAAAGGAGGAGGAGGAAACA (COX15) MANE Select NP_510870.1:n.396-29_396-28insAAAAAAGGAGG...
NR_164009.1:n.474-112_474-111insAAAAAAGGAGGAGGAGGAAACA (COX15)