Canonical Allele Identifier: CA11406838

Gene: FHIT

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.59995799T>C , CM000665.2:g.59995799T>C	GRCh38
NC_000003.11:g.59981525T>C , CM000665.1:g.59981525T>C	GRCh37
NC_000003.10:g.59956565T>C	NCBI36
NG_007551.1:g.1260609A>G
NG_007551.2:g.1260661A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492590.6:c.279+15572A>G MANE Select	ENSP00000418582.1:n.279+15572A>G
ENST00000466788.1:n.306+15572A>G
ENST00000468189.5:c.279+15572A>G	ENSP00000417480.1:n.279+15572A>G
ENST00000476844.5:c.279+15572A>G	ENSP00000417557.1:n.279+15572A>G
ENST00000492590.5:c.279+15572A>G	ENSP00000418582.1:n.279+15572A>G
NM_001166243.1:c.279+15572A>G	NP_001159715.1:n.279+15572A>G
NM_002012.2:c.279+15572A>G	NP_002003.1:n.279+15572A>G
XM_011533481.1:c.279+15572A>G	XP_011531783.1:n.279+15572A>G
XM_011533482.1:c.279+15572A>G	XP_011531784.1:n.279+15572A>G
XM_011533483.1:c.279+15572A>G	XP_011531785.1:n.279+15572A>G
XM_011533484.1:c.279+15572A>G	XP_011531786.1:n.279+15572A>G
XM_011533485.1:c.279+15572A>G	XP_011531787.1:n.279+15572A>G
XM_011533486.1:c.279+15572A>G	XP_011531788.1:n.279+15572A>G
NM_001166243.2:c.279+15572A>G	NP_001159715.1:n.279+15572A>G
NM_001320899.1:c.279+15572A>G	NP_001307828.1:n.279+15572A>G
NM_001320900.1:c.279+15572A>G	NP_001307829.1:n.279+15572A>G
NM_001320901.1:c.111+15572A>G	NP_001307830.1:n.111+15572A>G
NM_001354589.1:c.279+15572A>G	NP_001341518.1:n.279+15572A>G
NM_001354590.1:c.279+15572A>G	NP_001341519.1:n.279+15572A>G
NM_002012.3:c.279+15572A>G	NP_002003.1:n.279+15572A>G
NR_135491.1:n.593+15572A>G
XM_017005880.2:c.280-640A>G	XP_016861369.1:n.280-640A>G
XM_017005881.2:c.280-640A>G	XP_016861370.1:n.280-640A>G
XM_017005882.2:c.280-12054A>G	XP_016861371.1:n.280-12054A>G
XM_017005883.1:c.280-640A>G	XP_016861372.1:n.280-640A>G
XM_017005884.1:c.280-640A>G	XP_016861373.1:n.280-640A>G
XM_017005885.2:c.37-640A>G	XP_016861374.1:n.37-640A>G
XM_017005886.2:c.37-640A>G	XP_016861375.1:n.37-640A>G
NM_002012.4:c.279+15572A>G MANE Select	NP_002003.1:n.279+15572A>G
NM_001166243.3:c.279+15572A>G	NP_001159715.1:n.279+15572A>G
NM_001320899.2:c.279+15572A>G	NP_001307828.1:n.279+15572A>G
NM_001320900.2:c.279+15572A>G	NP_001307829.1:n.279+15572A>G
NM_001320901.2:c.111+15572A>G	NP_001307830.1:n.111+15572A>G
NM_001354589.2:c.279+15572A>G	NP_001341518.1:n.279+15572A>G
NM_001354590.2:c.279+15572A>G	NP_001341519.1:n.279+15572A>G
NR_135491.2:n.375+15572A>G