Canonical Allele Identifier: CA395618952

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902291C>T , CM000678.2:g.30902291C>T	GRCh38
NC_000016.9:g.30913612C>T , CM000678.1:g.30913612C>T	GRCh37
NC_000016.8:g.30821113C>T	NCBI36
NG_009171.1:g.10685C>T , LRG_408:g.10685C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.358C>T MANE Select	ENSP00000279804.2:p.Arg120Cys
ENST00000279804.2:c.358C>T	ENSP00000279804.2:p.Arg120Cys
ENST00000395019.3:c.355C>T	ENSP00000378465.3:p.Arg119Cys
NM_001142544.1:c.355C>T	NP_001136016.1:p.Arg119Cys
NM_001330.3:c.358C>T , LRG_408t1:c.358C>T	NP_001321.1:p.Arg120Cys
XM_011545759.1:c.424C>T	XP_011544061.1:p.Arg142Cys
XM_011545760.1:c.382C>T	XP_011544062.1:p.Arg128Cys
XM_011545759.2:c.424C>T	XP_011544061.1:p.Arg142Cys
XM_011545760.2:c.382C>T	XP_011544062.1:p.Arg128Cys
NM_001142544.2:c.355C>T	NP_001136016.1:p.Arg119Cys
NM_001142544.3:c.355C>T	NP_001136016.1:p.Arg119Cys
NM_001330.5:c.358C>T MANE Select	NP_001321.1:p.Arg120Cys
NR_165660.1:n.496C>T