Canonical Allele Identifier: CA280531304

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902430G>C , CM000678.2:g.30902430G>C	GRCh38
NC_000016.9:g.30913751G>C , CM000678.1:g.30913751G>C	GRCh37
NC_000016.8:g.30821252G>C	NCBI36
NG_009171.1:g.10824G>C , LRG_408:g.10824G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.497G>C MANE Select	ENSP00000279804.2:p.Gly166Ala
ENST00000279804.2:c.497G>C	ENSP00000279804.2:p.Gly166Ala
ENST00000395019.3:c.494G>C	ENSP00000378465.3:p.Gly165Ala
NM_001142544.1:c.494G>C	NP_001136016.1:p.Gly165Ala
NM_001330.3:c.497G>C , LRG_408t1:c.497G>C	NP_001321.1:p.Gly166Ala
XM_011545759.1:c.563G>C	XP_011544061.1:p.Gly188Ala
XM_011545760.1:c.521G>C	XP_011544062.1:p.Gly174Ala
XM_011545759.2:c.563G>C	XP_011544061.1:p.Gly188Ala
XM_011545760.2:c.521G>C	XP_011544062.1:p.Gly174Ala
NM_001142544.2:c.494G>C	NP_001136016.1:p.Gly165Ala
NM_001142544.3:c.494G>C	NP_001136016.1:p.Gly165Ala
NM_001330.5:c.497G>C MANE Select	NP_001321.1:p.Gly166Ala
NR_165660.1:n.635G>C