Canonical Allele Identifier: CA2216764889

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30902279_30902308del , CM000678.2:g.30902279_30902308del	GRCh38
NC_000016.9:g.30913600_30913629del , CM000678.1:g.30913600_30913629del	GRCh37
NC_000016.8:g.30821101_30821130del	NCBI36
NG_009171.1:g.10673_10702del , LRG_408:g.10673_10702del

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.346_375del MANE Select	NP_001321.1:p.Pro116_Ala125del
ENST00000279804.3:c.346_375del MANE Select	ENSP00000279804.2:p.Pro116_Ala125del
NM_001142544.1:c.343_372del	NP_001136016.1:p.Pro115_Ala124del
NM_001142544.2:c.343_372del	NP_001136016.1:p.Pro115_Ala124del
NM_001142544.3:c.343_372del	NP_001136016.1:p.Pro115_Ala124del
NM_001330.3:c.346_375del , LRG_408t1:c.346_375del	NP_001321.1:p.Pro116_Ala125del
NR_165660.1:n.484_513del
ENST00000279804.2:c.346_375del	ENSP00000279804.2:p.Pro116_Ala125del
ENST00000395019.3:c.343_372del	ENSP00000378465.3:p.Pro115_Ala124del
XM_011545759.1:c.412_441del	XP_011544061.1:p.Pro138_Ala147del
XM_011545759.2:c.412_441del	XP_011544061.1:p.Pro138_Ala147del
XM_011545760.1:c.370_399del	XP_011544062.1:p.Pro124_Ala133del
XM_011545760.2:c.370_399del	XP_011544062.1:p.Pro124_Ala133del