Canonical Allele Identifier: CA395618242

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902095C>A , CM000678.2:g.30902095C>A	GRCh38
NC_000016.9:g.30913416C>A , CM000678.1:g.30913416C>A	GRCh37
NC_000016.8:g.30820917C>A	NCBI36
NG_009171.1:g.10489C>A , LRG_408:g.10489C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.162C>A MANE Select	NP_001321.1:p.Asp54Glu
ENST00000279804.3:c.162C>A MANE Select	ENSP00000279804.2:p.Asp54Glu
NM_001142544.1:c.159C>A	NP_001136016.1:p.Asp53Glu
NM_001142544.2:c.159C>A	NP_001136016.1:p.Asp53Glu
NM_001142544.3:c.159C>A	NP_001136016.1:p.Asp53Glu
NM_001330.3:c.162C>A , LRG_408t1:c.162C>A	NP_001321.1:p.Asp54Glu
NR_165660.1:n.300C>A
ENST00000279804.2:c.162C>A	ENSP00000279804.2:p.Asp54Glu
ENST00000395019.3:c.159C>A	ENSP00000378465.3:p.Asp53Glu
XM_011545759.1:c.228C>A	XP_011544061.1:p.Asp76Glu
XM_011545759.2:c.228C>A	XP_011544061.1:p.Asp76Glu
XM_011545760.1:c.186C>A	XP_011544062.1:p.Asp62Glu
XM_011545760.2:c.186C>A	XP_011544062.1:p.Asp62Glu