Canonical Allele Identifier: CA2580091508

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902435_30902437del , CM000678.2:g.30902435_30902437del	GRCh38
NC_000016.9:g.30913756_30913758del , CM000678.1:g.30913756_30913758del	GRCh37
NC_000016.8:g.30821257_30821259del	NCBI36
NG_009171.1:g.10829_10831del , LRG_408:g.10829_10831del

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.502_504del MANE Select	NP_001321.1:p.Phe168del
ENST00000279804.3:c.502_504del MANE Select	ENSP00000279804.2:p.Phe168del
NM_001142544.1:c.499_501del	NP_001136016.1:p.Phe167del
NM_001142544.2:c.499_501del	NP_001136016.1:p.Phe167del
NM_001142544.3:c.499_501del	NP_001136016.1:p.Phe167del
NM_001330.3:c.502_504del , LRG_408t1:c.502_504del	NP_001321.1:p.Phe168del
NR_165660.1:n.640_642del
ENST00000279804.2:c.502_504del	ENSP00000279804.2:p.Phe168del
ENST00000395019.3:c.499_501del	ENSP00000378465.3:p.Phe167del
XM_011545759.1:c.568_570del	XP_011544061.1:p.Phe190del
XM_011545759.2:c.568_570del	XP_011544061.1:p.Phe190del
XM_011545760.1:c.526_528del	XP_011544062.1:p.Phe176del
XM_011545760.2:c.526_528del	XP_011544062.1:p.Phe176del