Canonical Allele Identifier: CA14281325

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30901874G>C , CM000678.2:g.30901874G>C	GRCh38
NC_000016.9:g.30913195G>C , CM000678.1:g.30913195G>C	GRCh37
NC_000016.8:g.30820696G>C	NCBI36
NG_009171.1:g.10268G>C , LRG_408:g.10268G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.145-204G>C MANE Select	NP_001321.1:n.145-204G>C
ENST00000279804.3:c.145-204G>C MANE Select	ENSP00000279804.2:n.145-204G>C
NM_001142544.1:c.142-204G>C	NP_001136016.1:n.142-204G>C
NM_001142544.2:c.142-204G>C	NP_001136016.1:n.142-204G>C
NM_001142544.3:c.142-204G>C	NP_001136016.1:n.142-204G>C
NM_001330.3:c.145-204G>C , LRG_408t1:c.145-204G>C	NP_001321.1:n.145-204G>C
NR_165660.1:n.283-204G>C
ENST00000279804.2:c.145-204G>C	ENSP00000279804.2:n.145-204G>C
ENST00000395019.3:c.142-204G>C	ENSP00000378465.3:n.142-204G>C
XM_011545759.1:c.211-204G>C	XP_011544061.1:n.211-204G>C
XM_011545759.2:c.211-204G>C	XP_011544061.1:n.211-204G>C
XM_011545760.1:c.169-204G>C	XP_011544062.1:n.169-204G>C
XM_011545760.2:c.169-204G>C	XP_011544062.1:n.169-204G>C