Canonical Allele Identifier: CA14516804

Gene: CTIF

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.48611704C>G , CM000680.2:g.48611704C>G	GRCh38
NC_000018.9:g.46138075C>G , CM000680.1:g.46138075C>G	GRCh37
NC_000018.8:g.44392073C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256413.8:c.-28-7834C>G MANE Select	ENSP00000256413.3:n.-28-7834C>G
ENST00000256413.7:c.-28-7834C>G	ENSP00000256413.3:n.-28-7834C>G
ENST00000382998.8:c.-28-7834C>G	ENSP00000372459.3:n.-28-7834C>G
ENST00000587752.5:c.-28-7834C>G	ENSP00000465405.2:n.-28-7834C>G
ENST00000588345.1:c.-28-7834C>G	ENSP00000467957.1:n.-28-7834C>G
ENST00000591387.5:c.-28-7834C>G	ENSP00000467425.1:n.-28-7834C>G
ENST00000591412.5:c.-28-7834C>G	ENSP00000467965.1:n.-28-7834C>G
NM_001142397.1:c.-28-7834C>G	NP_001135869.1:n.-28-7834C>G
NM_014772.2:c.-28-7834C>G	NP_055587.1:n.-28-7834C>G
XM_005258392.3:c.-28-7834C>G	XP_005258449.1:n.-28-7834C>G
XM_006722583.2:c.-28-7834C>G	XP_006722646.1:n.-28-7834C>G
XM_006722585.2:c.-28-7834C>G	XP_006722648.1:n.-28-7834C>G
XM_006722586.2:c.-28-7834C>G	XP_006722649.1:n.-28-7834C>G
XM_006722587.2:c.-28-7834C>G	XP_006722650.1:n.-28-7834C>G
XM_006722588.2:c.-28-7834C>G	XP_006722651.1:n.-28-7834C>G
XM_006722589.2:c.-28-7834C>G	XP_006722652.1:n.-28-7834C>G
XM_011526279.1:c.-28-7834C>G	XP_011524581.1:n.-28-7834C>G
XM_011526280.1:c.-28-7834C>G	XP_011524582.1:n.-28-7834C>G
XM_005258392.4:c.-28-7834C>G	XP_005258449.1:n.-28-7834C>G
XM_006722583.3:c.-28-7834C>G	XP_006722646.1:n.-28-7834C>G
XM_006722586.3:c.-28-7834C>G	XP_006722649.1:n.-28-7834C>G
XM_006722587.3:c.-28-7834C>G	XP_006722650.1:n.-28-7834C>G
XM_006722588.4:c.-28-7834C>G	XP_006722651.1:n.-28-7834C>G
XM_011526279.2:c.-28-7834C>G	XP_011524581.1:n.-28-7834C>G
XM_017026100.1:c.-28-7834C>G	XP_016881589.1:n.-28-7834C>G
XM_017026101.1:c.-28-7834C>G	XP_016881590.1:n.-28-7834C>G
XM_017026102.1:c.-28-7834C>G	XP_016881591.1:n.-28-7834C>G
NM_014772.3:c.-28-7834C>G MANE Select	NP_055587.1:n.-28-7834C>G
NM_001142397.2:c.-28-7834C>G	NP_001135869.1:n.-28-7834C>G