Canonical Allele Identifier: CA494915737

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902380G>T , CM000678.2:g.30902380G>T	GRCh38
NC_000016.9:g.30913701G>T , CM000678.1:g.30913701G>T	GRCh37
NC_000016.8:g.30821202G>T	NCBI36
NG_009171.1:g.10774G>T , LRG_408:g.10774G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.447G>T MANE Select	ENSP00000279804.2:p.Gly149=
ENST00000279804.2:c.447G>T	ENSP00000279804.2:p.Gly149=
ENST00000395019.3:c.444G>T	ENSP00000378465.3:p.Gly148=
NM_001142544.1:c.444G>T	NP_001136016.1:p.Gly148=
NM_001330.3:c.447G>T , LRG_408t1:c.447G>T	NP_001321.1:p.Gly149=
XM_011545759.1:c.513G>T	XP_011544061.1:p.Gly171=
XM_011545760.1:c.471G>T	XP_011544062.1:p.Gly157=
XM_011545759.2:c.513G>T	XP_011544061.1:p.Gly171=
XM_011545760.2:c.471G>T	XP_011544062.1:p.Gly157=
NM_001142544.2:c.444G>T	NP_001136016.1:p.Gly148=
NM_001142544.3:c.444G>T	NP_001136016.1:p.Gly148=
NM_001330.5:c.447G>T MANE Select	NP_001321.1:p.Gly149=
NR_165660.1:n.585G>T