Canonical Allele Identifier: CA1931477922

Gene: CUTC COX15

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99732646T= , CM000672.2:g.99732646T=	GRCh38
NC_000010.10:g.101492403T= , CM000672.1:g.101492403T=	GRCh37
NC_000010.9:g.101482393T=	NCBI36
NG_008986.1:g.5021A= , LRG_406:g.5021A=

Transcript Alleles

HGVS	Amino-acid Change
NM_015960.3:c.61+237T= (CUTC) MANE Select	NP_057044.2:n.61+237T=
ENST00000370476.10:c.61+237T= (CUTC) MANE Select	ENSP00000359507.5:n.61+237T=
NM_001320974.1:c.-597A= (COX15)	NP_001307903.1:n.-597A=
NM_001320975.1:c.-597A= (COX15)	NP_001307904.1:n.-597A=
NM_001320976.1:c.-1051A= (COX15)	NP_001307905.1:n.-1051A=
NM_004376.5:c.-597A= , LRG_406t2:c.-597A= (COX15)	NP_004367.2:n.-597A=
NM_004376.6:c.-597A= (COX15)	NP_004367.2:n.-597A=
NM_015960.2:c.61+237T= (CUTC)	NP_057044.2:n.61+237T=
NM_078470.4:c.-597A= , LRG_406t1:c.-597A= (COX15)	NP_510870.1:n.-597A=
NM_078470.5:c.-597A= (COX15)	NP_510870.1:n.-597A=
ENST00000370472.4:c.-129+86T= (CUTC)	ENSP00000359503.4:n.-129+86T=
ENST00000370476.9:c.61+237T= (CUTC)	ENSP00000359507.5:n.61+237T=
ENST00000471520.5:c.61+237T= (CUTC)	ENSP00000433900.1:n.61+237T=
ENST00000493385.5:n.310-3600T= (CUTC)