Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99720978G>A , CM000672.2:g.99720978G>A	GRCh38
NC_000010.10:g.101480735G>A , CM000672.1:g.101480735G>A	GRCh37
NC_000010.9:g.101470725G>A	NCBI36
NG_008986.1:g.16689C>T , LRG_406:g.16689C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_078470.6:c.832+9C>T (COX15) MANE Select	NP_510870.1:n.832+9C>T
ENST00000016171.6:c.832+9C>T (COX15) MANE Select	ENSP00000016171.6:n.832+9C>T
NM_001320974.1:c.832+9C>T (COX15)	NP_001307903.1:n.832+9C>T
NM_001320974.2:c.832+9C>T (COX15)	NP_001307903.1:n.832+9C>T
NM_001320975.1:c.832+9C>T (COX15)	NP_001307904.1:n.832+9C>T
NM_001320975.2:c.832+9C>T (COX15)	NP_001307904.1:n.832+9C>T
NM_001320976.1:c.295+9C>T (COX15)	NP_001307905.1:n.295+9C>T
NM_001320976.2:c.295+9C>T (COX15)	NP_001307905.1:n.295+9C>T
NM_001372024.1:c.832+9C>T (COX15)	NP_001358953.1:n.832+9C>T
NM_001372025.1:c.832+9C>T (COX15)	NP_001358954.1:n.832+9C>T
NM_001372026.1:c.805+36C>T (COX15)	NP_001358955.1:n.805+36C>T
NM_001372027.1:c.832+9C>T (COX15)	NP_001358956.1:n.832+9C>T
NM_001372028.1:c.832+9C>T (COX15)	NP_001358957.1:n.832+9C>T
NM_004376.5:c.832+9C>T , LRG_406t2:c.832+9C>T (COX15)	NP_004367.2:n.832+9C>T
NM_004376.6:c.832+9C>T (COX15)	NP_004367.2:n.832+9C>T
NM_004376.7:c.832+9C>T (COX15)	NP_004367.2:n.832+9C>T
NM_078470.4:c.832+9C>T , LRG_406t1:c.832+9C>T (COX15)	NP_510870.1:n.832+9C>T
NM_078470.5:c.832+9C>T (COX15)	NP_510870.1:n.832+9C>T
NR_164009.1:n.827+9C>T (COX15)
ENST00000016171.5:c.832+9C>T (COX15)	ENSP00000016171.5:n.832+9C>T
ENST00000370483.9:c.832+9C>T (COX15)	ENSP00000359514.5:n.832+9C>T
ENST00000493385.5:n.117-1940G>A (CUTC)
ENST00000649102.1:c.*191+9C>T	ENSP00000497114.1:n.*191+9C>T
XM_005269539.3:c.832+9C>T (COX15)	XP_005269596.1:n.832+9C>T
XM_006717633.2:c.832+9C>T (COX15)	XP_006717696.1:n.832+9C>T
XM_006717634.2:c.832+9C>T (COX15)	XP_006717697.1:n.832+9C>T
XM_006717634.3:c.832+9C>T (COX15)	XP_006717697.1:n.832+9C>T
XM_011539298.1:c.832+9C>T (COX15)	XP_011537600.1:n.832+9C>T
XM_011539298.2:c.832+9C>T (COX15)	XP_011537600.1:n.832+9C>T