Canonical Allele Identifier: CA658658465

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902278_30902279dup , CM000678.2:g.30902278_30902279dup	GRCh38
NC_000016.9:g.30913599_30913600dup , CM000678.1:g.30913599_30913600dup	GRCh37
NC_000016.8:g.30821100_30821101dup	NCBI36
NG_009171.1:g.10672_10673dup , LRG_408:g.10672_10673dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.345_346dup MANE Select	NP_001321.1:p.Pro116ArgfsTer?
ENST00000279804.3:c.345_346dup MANE Select	ENSP00000279804.2:p.Pro116ArgfsTer?
NM_001142544.1:c.342_343dup	NP_001136016.1:p.Pro115ArgfsTer?
NM_001142544.2:c.342_343dup	NP_001136016.1:p.Pro115ArgfsTer?
NM_001142544.3:c.342_343dup	NP_001136016.1:p.Pro115ArgfsTer?
NM_001330.3:c.345_346dup , LRG_408t1:c.345_346dup	NP_001321.1:p.Pro116ArgfsTer?
NR_165660.1:n.483_484dup
ENST00000279804.2:c.345_346dup	ENSP00000279804.2:p.Pro116ArgfsTer?
ENST00000395019.3:c.342_343dup	ENSP00000378465.3:p.Pro115ArgfsTer?
XM_011545759.1:c.411_412dup	XP_011544061.1:p.Pro138ArgfsTer?
XM_011545759.2:c.411_412dup	XP_011544061.1:p.Pro138ArgfsTer?
XM_011545760.1:c.369_370dup	XP_011544062.1:p.Pro124ArgfsTer?
XM_011545760.2:c.369_370dup	XP_011544062.1:p.Pro124ArgfsTer?