Canonical Allele Identifier: CA1931472439

Gene: COX15 CUTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99727080C= , CM000672.2:g.99727080C=	GRCh38
NC_000010.10:g.101486837C= , CM000672.1:g.101486837C=	GRCh37
NC_000010.9:g.101476827C=	NCBI36
NG_008986.1:g.10587G= , LRG_406:g.10587G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000016171.6:c.470G= (COX15) MANE Select	ENSP00000016171.6:p.Arg157=
ENST00000649102.1:c.396-9G=	ENSP00000497114.1:n.396-9G=
ENST00000016171.5:c.470G= (COX15)	ENSP00000016171.5:p.Arg157=
ENST00000370483.9:c.470G= (COX15)	ENSP00000359514.5:p.Arg157=
ENST00000493385.5:n.309+3970C= (CUTC)
NM_004376.5:c.470G= , LRG_406t2:c.470G= (COX15)	NP_004367.2:p.Arg157=
NM_078470.4:c.470G= , LRG_406t1:c.470G= (COX15)	NP_510870.1:p.Arg157=
XM_005269539.3:c.470G= (COX15)	XP_005269596.1:p.Arg157=
XM_006717633.2:c.470G= (COX15)	XP_006717696.1:p.Arg157=
XM_006717634.2:c.470G= (COX15)	XP_006717697.1:p.Arg157=
XM_011539298.1:c.470G= (COX15)	XP_011537600.1:p.Arg157=
NM_001320974.1:c.470G= (COX15)	NP_001307903.1:p.Arg157=
NM_001320975.1:c.470G= (COX15)	NP_001307904.1:p.Arg157=
NM_001320976.1:c.-59-9G= (COX15)	NP_001307905.1:n.-59-9G=
NM_004376.6:c.470G= (COX15)	NP_004367.2:p.Arg157=
NM_078470.5:c.470G= (COX15)	NP_510870.1:p.Arg157=
XM_006717634.3:c.470G= (COX15)	XP_006717697.1:p.Arg157=
XM_011539298.2:c.470G= (COX15)	XP_011537600.1:p.Arg157=
NM_001320974.2:c.470G= (COX15)	NP_001307903.1:p.Arg157=
NM_001320975.2:c.470G= (COX15)	NP_001307904.1:p.Arg157=
NM_001320976.2:c.-59-9G= (COX15)	NP_001307905.1:n.-59-9G=
NM_001372024.1:c.470G= (COX15)	NP_001358953.1:p.Arg157=
NM_001372025.1:c.470G= (COX15)	NP_001358954.1:p.Arg157=
NM_001372026.1:c.470G= (COX15)	NP_001358955.1:p.Arg157=
NM_001372027.1:c.470G= (COX15)	NP_001358956.1:p.Arg157=
NM_001372028.1:c.470G= (COX15)	NP_001358957.1:p.Arg157=
NM_004376.7:c.470G= (COX15)	NP_004367.2:p.Arg157=
NM_078470.6:c.470G= (COX15) MANE Select	NP_510870.1:p.Arg157=
NR_164009.1:n.474-9G= (COX15)