Canonical Allele Identifier: CA299896350

Gene: CTIF

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.48810331A>T , CM000680.2:g.48810331A>T	GRCh38
NC_000018.9:g.46336702A>T , CM000680.1:g.46336702A>T	GRCh37
NC_000018.8:g.44590700A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256413.8:c.1372-6890A>T MANE Select	ENSP00000256413.3:n.1372-6890A>T
ENST00000256413.7:c.1372-6890A>T	ENSP00000256413.3:n.1372-6890A>T
ENST00000382998.8:c.1378-6890A>T	ENSP00000372459.3:n.1378-6890A>T
ENST00000587860.1:n.1509-6890A>T
NM_001142397.1:c.1378-6890A>T	NP_001135869.1:n.1378-6890A>T
NM_014772.2:c.1372-6890A>T	NP_055587.1:n.1372-6890A>T
XM_005258392.3:c.1426-6890A>T	XP_005258449.1:n.1426-6890A>T
XM_006722583.2:c.1426-6890A>T	XP_006722646.1:n.1426-6890A>T
XM_006722585.2:c.1426-6890A>T	XP_006722648.1:n.1426-6890A>T
XM_006722586.2:c.1420-6890A>T	XP_006722649.1:n.1420-6890A>T
XM_006722587.2:c.1378-6890A>T	XP_006722650.1:n.1378-6890A>T
XM_006722588.2:c.1378-6890A>T	XP_006722651.1:n.1378-6890A>T
XM_006722589.2:c.1378-6890A>T	XP_006722652.1:n.1378-6890A>T
XM_011526278.1:c.1303-6890A>T	XP_011524580.1:n.1303-6890A>T
XM_011526279.1:c.1372-6890A>T	XP_011524581.1:n.1372-6890A>T
XM_005258392.4:c.1426-6890A>T	XP_005258449.1:n.1426-6890A>T
XM_006722583.3:c.1426-6890A>T	XP_006722646.1:n.1426-6890A>T
XM_006722586.3:c.1420-6890A>T	XP_006722649.1:n.1420-6890A>T
XM_006722587.3:c.1378-6890A>T	XP_006722650.1:n.1378-6890A>T
XM_006722588.4:c.1378-6890A>T	XP_006722651.1:n.1378-6890A>T
XM_011526278.3:c.1303-6890A>T	XP_011524580.1:n.1303-6890A>T
XM_011526279.2:c.1372-6890A>T	XP_011524581.1:n.1372-6890A>T
XM_017026100.1:c.1426-6890A>T	XP_016881589.1:n.1426-6890A>T
XM_017026101.1:c.1426-6890A>T	XP_016881590.1:n.1426-6890A>T
XM_017026102.1:c.1378-6890A>T	XP_016881591.1:n.1378-6890A>T
NM_014772.3:c.1372-6890A>T MANE Select	NP_055587.1:n.1372-6890A>T
NM_001142397.2:c.1378-6890A>T	NP_001135869.1:n.1378-6890A>T