Canonical Allele Identifier: CA1931452036

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99713325_99713326delinsAT , CM000672.2:g.99713325_99713326delinsAT	GRCh38
NC_000010.10:g.101473082_101473083delinsAT , CM000672.1:g.101473082_101473083delinsAT	GRCh37
NC_000010.9:g.101463072_101463073delinsAT	NCBI36
NG_008986.1:g.24341_24342delinsAT , LRG_406:g.24341_24342delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000016171.6:c.*1261_*1262delinsAT (COX15) MANE Select	ENSP00000016171.6:n.*1261_*1262delinsAT
ENST00000649102.1:c.*460+3022_*460+3023delinsAT	ENSP00000497114.1:n.*460+3022_*460+3023delinsAT
ENST00000370483.9:c.*88_*89delinsAT (COX15)	ENSP00000359514.5:n.*88_*89delinsAT
ENST00000493385.5:n.117-9593_117-9592delinsAT (CUTC)
NM_004376.5:c.*88_*89delinsAT , LRG_406t2:c.*88_*89delinsAT (COX15)	NP_004367.2:n.*88_*89delinsAT
NM_078470.4:c.*1261_*1262delinsAT , LRG_406t1:c.*1261_*1262delinsAT (COX15)	NP_510870.1:n.*1261_*1262delinsAT
XM_005269539.3:c.1101+3022_1101+3023delinsAT (COX15)	XP_005269596.1:n.1101+3022_1101+3023delinsAT
XM_006717633.2:c.*1442_*1443delinsAT (COX15)	XP_006717696.1:n.*1442_*1443delinsAT
XM_006717634.2:c.*49+3022_*49+3023delinsAT (COX15)	XP_006717697.1:n.*49+3022_*49+3023delinsAT
NM_001320974.1:c.1101+3022_1101+3023delinsAT (COX15)	NP_001307903.1:n.1101+3022_1101+3023delinsAT
NM_001320975.1:c.*1442_*1443delinsAT (COX15)	NP_001307904.1:n.*1442_*1443delinsAT
NM_001320976.1:c.*1261_*1262delinsAT (COX15)	NP_001307905.1:n.*1261_*1262delinsAT
NM_004376.6:c.*88_*89delinsAT (COX15)	NP_004367.2:n.*88_*89delinsAT
NM_078470.5:c.*1261_*1262delinsAT (COX15)	NP_510870.1:n.*1261_*1262delinsAT
XM_006717634.3:c.*49+3022_*49+3023delinsAT (COX15)	XP_006717697.1:n.*49+3022_*49+3023delinsAT
XM_011539298.2:c.*203_*204delinsAT (COX15)	XP_011537600.1:n.*203_*204delinsAT
NM_001320974.2:c.1101+3022_1101+3023delinsAT (COX15)	NP_001307903.1:n.1101+3022_1101+3023delinsAT
NM_001320975.2:c.*1442_*1443delinsAT (COX15)	NP_001307904.1:n.*1442_*1443delinsAT
NM_001320976.2:c.*1261_*1262delinsAT (COX15)	NP_001307905.1:n.*1261_*1262delinsAT
NM_001372024.1:c.*480_*481delinsAT (COX15)	NP_001358953.1:n.*480_*481delinsAT
NM_001372025.1:c.*1261_*1262delinsAT (COX15)	NP_001358954.1:n.*1261_*1262delinsAT
NM_001372026.1:c.*1261_*1262delinsAT (COX15)	NP_001358955.1:n.*1261_*1262delinsAT
NM_001372027.1:c.*1365_*1366delinsAT (COX15)	NP_001358956.1:n.*1365_*1366delinsAT
NM_001372028.1:c.*688_*689delinsAT (COX15)	NP_001358957.1:n.*688_*689delinsAT
NM_004376.7:c.*88_*89delinsAT (COX15)	NP_004367.2:n.*88_*89delinsAT
NM_078470.6:c.*1261_*1262delinsAT (COX15) MANE Select	NP_510870.1:n.*1261_*1262delinsAT
NR_164009.1:n.2334_2335delinsAT (COX15)