Canonical Allele Identifier: CA494915805

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902152C>G , CM000678.2:g.30902152C>G	GRCh38
NC_000016.9:g.30913473C>G , CM000678.1:g.30913473C>G	GRCh37
NC_000016.8:g.30820974C>G	NCBI36
NG_009171.1:g.10546C>G , LRG_408:g.10546C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.219C>G MANE Select	ENSP00000279804.2:p.Ala73=
ENST00000279804.2:c.219C>G	ENSP00000279804.2:p.Ala73=
ENST00000395019.3:c.216C>G	ENSP00000378465.3:p.Ala72=
NM_001142544.1:c.216C>G	NP_001136016.1:p.Ala72=
NM_001330.3:c.219C>G , LRG_408t1:c.219C>G	NP_001321.1:p.Ala73=
XM_011545759.1:c.285C>G	XP_011544061.1:p.Ala95=
XM_011545760.1:c.243C>G	XP_011544062.1:p.Ala81=
XM_011545759.2:c.285C>G	XP_011544061.1:p.Ala95=
XM_011545760.2:c.243C>G	XP_011544062.1:p.Ala81=
NM_001142544.2:c.216C>G	NP_001136016.1:p.Ala72=
NM_001142544.3:c.216C>G	NP_001136016.1:p.Ala72=
NM_001330.5:c.219C>G MANE Select	NP_001321.1:p.Ala73=
NR_165660.1:n.357C>G