Canonical Allele Identifier: CA8015478

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30899510G>T , CM000678.2:g.30899510G>T	GRCh38
NC_000016.9:g.30910831G>T , CM000678.1:g.30910831G>T	GRCh37
NC_000016.8:g.30818332G>T	NCBI36
NG_009171.1:g.7904G>T , LRG_408:g.7904G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.121G>T MANE Select	ENSP00000279804.2:p.Ala41Ser
ENST00000279804.2:c.121G>T	ENSP00000279804.2:p.Ala41Ser
ENST00000395019.3:c.118G>T	ENSP00000378465.3:p.Ala40Ser
NM_001142544.1:c.118G>T	NP_001136016.1:p.Ala40Ser
NM_001330.3:c.121G>T , LRG_408t1:c.121G>T	NP_001321.1:p.Ala41Ser
XM_011545759.1:c.187G>T	XP_011544061.1:p.Ala63Ser
XM_011545760.1:c.145G>T	XP_011544062.1:p.Ala49Ser
XM_011545759.2:c.187G>T	XP_011544061.1:p.Ala63Ser
XM_011545760.2:c.145G>T	XP_011544062.1:p.Ala49Ser
NM_001142544.2:c.118G>T	NP_001136016.1:p.Ala40Ser
NM_001142544.3:c.118G>T	NP_001136016.1:p.Ala40Ser
NM_001330.5:c.121G>T MANE Select	NP_001321.1:p.Ala41Ser
NR_165660.1:n.259G>T