Canonical Allele Identifier: CA2216766921

Gene: CTF1

Genomic Alleles

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

Transcript Alleles

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