Canonical Allele Identifier: CA395618819
Gene: CTF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30902252C>A , CM000678.2:g.30902252C>A GRCh38
NC_000016.9:g.30913573C>A , CM000678.1:g.30913573C>A GRCh37
NC_000016.8:g.30821074C>A NCBI36
NG_009171.1:g.10646C>A , LRG_408:g.10646C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001330.5:c.319C>A MANE Select NP_001321.1:p.Arg107Ser
ENST00000279804.3:c.319C>A MANE Select ENSP00000279804.2:p.Arg107Ser
NM_001142544.1:c.316C>A NP_001136016.1:p.Arg106Ser
NM_001142544.2:c.316C>A NP_001136016.1:p.Arg106Ser
NM_001142544.3:c.316C>A NP_001136016.1:p.Arg106Ser
NM_001330.3:c.319C>A , LRG_408t1:c.319C>A NP_001321.1:p.Arg107Ser
NR_165660.1:n.457C>A
ENST00000279804.2:c.319C>A ENSP00000279804.2:p.Arg107Ser
ENST00000395019.3:c.316C>A ENSP00000378465.3:p.Arg106Ser
XM_011545759.1:c.385C>A XP_011544061.1:p.Arg129Ser
XM_011545759.2:c.385C>A XP_011544061.1:p.Arg129Ser
XM_011545760.1:c.343C>A XP_011544062.1:p.Arg115Ser
XM_011545760.2:c.343C>A XP_011544062.1:p.Arg115Ser