Canonical Allele Identifier: CA8015458

Gene: CTF1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30899402C>A , CM000678.2:g.30899402C>A	GRCh38
NC_000016.9:g.30910723C>A , CM000678.1:g.30910723C>A	GRCh37
NC_000016.8:g.30818224C>A	NCBI36
NG_009171.1:g.7796C>A , LRG_408:g.7796C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001330.5:c.26-13C>A MANE Select	NP_001321.1:n.26-13C>A
ENST00000279804.3:c.26-13C>A MANE Select	ENSP00000279804.2:n.26-13C>A
NM_001142544.1:c.26-16C>A	NP_001136016.1:n.26-16C>A
NM_001142544.2:c.26-16C>A	NP_001136016.1:n.26-16C>A
NM_001142544.3:c.26-16C>A	NP_001136016.1:n.26-16C>A
NM_001330.3:c.26-13C>A , LRG_408t1:c.26-13C>A	NP_001321.1:n.26-13C>A
NR_165660.1:n.151C>A
ENST00000279804.2:c.26-13C>A	ENSP00000279804.2:n.26-13C>A
ENST00000395019.3:c.26-16C>A	ENSP00000378465.3:n.26-16C>A
XM_011545759.1:c.92-13C>A	XP_011544061.1:n.92-13C>A
XM_011545759.2:c.92-13C>A	XP_011544061.1:n.92-13C>A
XM_011545760.1:c.50-13C>A	XP_011544062.1:n.50-13C>A
XM_011545760.2:c.50-13C>A	XP_011544062.1:n.50-13C>A