Canonical Allele Identifier: CA133720

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902207G>A , CM000678.2:g.30902207G>A	GRCh38
NC_000016.9:g.30913528G>A , CM000678.1:g.30913528G>A	GRCh37
NC_000016.8:g.30821029G>A	NCBI36
NG_009171.1:g.10601G>A , LRG_408:g.10601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.274G>A MANE Select	ENSP00000279804.2:p.Ala92Thr
ENST00000279804.2:c.274G>A	ENSP00000279804.2:p.Ala92Thr
ENST00000395019.3:c.271G>A	ENSP00000378465.3:p.Ala91Thr
NM_001142544.1:c.271G>A	NP_001136016.1:p.Ala91Thr
NM_001330.3:c.274G>A , LRG_408t1:c.274G>A	NP_001321.1:p.Ala92Thr
XM_011545759.1:c.340G>A	XP_011544061.1:p.Ala114Thr
XM_011545760.1:c.298G>A	XP_011544062.1:p.Ala100Thr
XM_011545759.2:c.340G>A	XP_011544061.1:p.Ala114Thr
XM_011545760.2:c.298G>A	XP_011544062.1:p.Ala100Thr
NM_001142544.2:c.271G>A	NP_001136016.1:p.Ala91Thr
NM_001142544.3:c.271G>A	NP_001136016.1:p.Ala91Thr
NM_001330.5:c.274G>A MANE Select	NP_001321.1:p.Ala92Thr
NR_165660.1:n.412G>A