Canonical Allele Identifier: CA2216766929

Gene: CTF1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30903305T>A , CM000678.2:g.30903305T>A	GRCh38
NC_000016.9:g.30914626T>A , CM000678.1:g.30914626T>A	GRCh37
NC_000016.8:g.30822127T>A	NCBI36
NG_009171.1:g.11699T>A , LRG_408:g.11699T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279804.3:c.*766T>A MANE Select	ENSP00000279804.2:n.*766T>A
ENST00000279804.2:c.*766T>A	ENSP00000279804.2:n.*766T>A
ENST00000395019.3:c.*766T>A	ENSP00000378465.3:n.*766T>A
NM_001142544.1:c.*766T>A	NP_001136016.1:n.*766T>A
NM_001330.3:c.*766T>A , LRG_408t1:c.*766T>A	NP_001321.1:n.*766T>A
XM_011545759.1:c.*766T>A	XP_011544061.1:n.*766T>A
XM_011545760.1:c.*766T>A	XP_011544062.1:n.*766T>A
XM_011545759.2:c.*766T>A	XP_011544061.1:n.*766T>A
XM_011545760.2:c.*766T>A	XP_011544062.1:n.*766T>A
NM_001142544.2:c.*766T>A	NP_001136016.1:n.*766T>A
NM_001142544.3:c.*766T>A	NP_001136016.1:n.*766T>A
NM_001330.5:c.*766T>A MANE Select	NP_001321.1:n.*766T>A
NR_165660.1:n.1510T>A