Canonical Allele Identifier: CA395618741

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902228C>G , CM000678.2:g.30902228C>G	GRCh38
NC_000016.9:g.30913549C>G , CM000678.1:g.30913549C>G	GRCh37
NC_000016.8:g.30821050C>G	NCBI36
NG_009171.1:g.10622C>G , LRG_408:g.10622C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.295C>G MANE Select	ENSP00000279804.2:p.Pro99Ala
ENST00000279804.2:c.295C>G	ENSP00000279804.2:p.Pro99Ala
ENST00000395019.3:c.292C>G	ENSP00000378465.3:p.Pro98Ala
NM_001142544.1:c.292C>G	NP_001136016.1:p.Pro98Ala
NM_001330.3:c.295C>G , LRG_408t1:c.295C>G	NP_001321.1:p.Pro99Ala
XM_011545759.1:c.361C>G	XP_011544061.1:p.Pro121Ala
XM_011545760.1:c.319C>G	XP_011544062.1:p.Pro107Ala
XM_011545759.2:c.361C>G	XP_011544061.1:p.Pro121Ala
XM_011545760.2:c.319C>G	XP_011544062.1:p.Pro107Ala
NM_001142544.2:c.292C>G	NP_001136016.1:p.Pro98Ala
NM_001142544.3:c.292C>G	NP_001136016.1:p.Pro98Ala
NM_001330.5:c.295C>G MANE Select	NP_001321.1:p.Pro99Ala
NR_165660.1:n.433C>G