Canonical Allele Identifier: CA8015469

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30899464C>A , CM000678.2:g.30899464C>A	GRCh38
NC_000016.9:g.30910785C>A , CM000678.1:g.30910785C>A	GRCh37
NC_000016.8:g.30818286C>A	NCBI36
NG_009171.1:g.7858C>A , LRG_408:g.7858C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.75C>A MANE Select	ENSP00000279804.2:p.Ala25=
ENST00000279804.2:c.75C>A	ENSP00000279804.2:p.Ala25=
ENST00000395019.3:c.72C>A	ENSP00000378465.3:p.Ala24=
NM_001142544.1:c.72C>A	NP_001136016.1:p.Ala24=
NM_001330.3:c.75C>A , LRG_408t1:c.75C>A	NP_001321.1:p.Ala25=
XM_011545759.1:c.141C>A	XP_011544061.1:p.Ala47=
XM_011545760.1:c.99C>A	XP_011544062.1:p.Ala33=
XM_011545759.2:c.141C>A	XP_011544061.1:p.Ala47=
XM_011545760.2:c.99C>A	XP_011544062.1:p.Ala33=
NM_001142544.2:c.72C>A	NP_001136016.1:p.Ala24=
NM_001142544.3:c.72C>A	NP_001136016.1:p.Ala24=
NM_001330.5:c.75C>A MANE Select	NP_001321.1:p.Ala25=
NR_165660.1:n.213C>A