Canonical Allele Identifier: CA395619630

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902469G>A , CM000678.2:g.30902469G>A	GRCh38
NC_000016.9:g.30913790G>A , CM000678.1:g.30913790G>A	GRCh37
NC_000016.8:g.30821291G>A	NCBI36
NG_009171.1:g.10863G>A , LRG_408:g.10863G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.536G>A MANE Select	NP_001321.1:p.Gly179Asp
ENST00000279804.3:c.536G>A MANE Select	ENSP00000279804.2:p.Gly179Asp
NM_001142544.1:c.533G>A	NP_001136016.1:p.Gly178Asp
NM_001142544.2:c.533G>A	NP_001136016.1:p.Gly178Asp
NM_001142544.3:c.533G>A	NP_001136016.1:p.Gly178Asp
NM_001330.3:c.536G>A , LRG_408t1:c.536G>A	NP_001321.1:p.Gly179Asp
NR_165660.1:n.674G>A
ENST00000279804.2:c.536G>A	ENSP00000279804.2:p.Gly179Asp
ENST00000395019.3:c.533G>A	ENSP00000378465.3:p.Gly178Asp
XM_011545759.1:c.602G>A	XP_011544061.1:p.Gly201Asp
XM_011545759.2:c.602G>A	XP_011544061.1:p.Gly201Asp
XM_011545760.1:c.560G>A	XP_011544062.1:p.Gly187Asp
XM_011545760.2:c.560G>A	XP_011544062.1:p.Gly187Asp