Canonical Allele Identifier: CA1368590729

Gene: FHIT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.60304223_60304224delinsAT , CM000665.2:g.60304223_60304224delinsAT	GRCh38
NC_000003.11:g.60289952_60289953delinsAT , CM000665.1:g.60289952_60289953delinsAT	GRCh37
NC_000003.10:g.60264992_60264993delinsAT	NCBI36
NG_007551.1:g.952181_952182delinsAT
NG_007551.2:g.952236_952237delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492590.6:c.103+232636_103+232637delinsAT MANE Select	ENSP00000418582.1:n.103+232636_103+232637delinsAT
ENST00000468189.5:c.103+232636_103+232637delinsAT	ENSP00000417480.1:n.103+232636_103+232637delinsAT
ENST00000476844.5:c.103+232636_103+232637delinsAT	ENSP00000417557.1:n.103+232636_103+232637delinsAT
ENST00000488467.5:c.103+232636_103+232637delinsAT	ENSP00000418596.1:n.103+232636_103+232637delinsAT
ENST00000492590.5:c.103+232636_103+232637delinsAT	ENSP00000418582.1:n.103+232636_103+232637delinsAT
NM_001166243.1:c.103+232636_103+232637delinsAT	NP_001159715.1:n.103+232636_103+232637delinsAT
NM_002012.2:c.103+232636_103+232637delinsAT	NP_002003.1:n.103+232636_103+232637delinsAT
XM_011533481.1:c.103+232636_103+232637delinsAT	XP_011531783.1:n.103+232636_103+232637delinsAT
XM_011533482.1:c.103+232636_103+232637delinsAT	XP_011531784.1:n.103+232636_103+232637delinsAT
XM_011533483.1:c.103+232636_103+232637delinsAT	XP_011531785.1:n.103+232636_103+232637delinsAT
XM_011533484.1:c.103+232636_103+232637delinsAT	XP_011531786.1:n.103+232636_103+232637delinsAT
XM_011533485.1:c.103+232636_103+232637delinsAT	XP_011531787.1:n.103+232636_103+232637delinsAT
XM_011533486.1:c.103+232636_103+232637delinsAT	XP_011531788.1:n.103+232636_103+232637delinsAT
NM_001166243.2:c.103+232636_103+232637delinsAT	NP_001159715.1:n.103+232636_103+232637delinsAT
NM_001320899.1:c.103+232636_103+232637delinsAT	NP_001307828.1:n.103+232636_103+232637delinsAT
NM_001320900.1:c.103+232636_103+232637delinsAT	NP_001307829.1:n.103+232636_103+232637delinsAT
NM_001354589.1:c.103+232636_103+232637delinsAT	NP_001341518.1:n.103+232636_103+232637delinsAT
NM_001354590.1:c.103+232636_103+232637delinsAT	NP_001341519.1:n.103+232636_103+232637delinsAT
NM_002012.3:c.103+232636_103+232637delinsAT	NP_002003.1:n.103+232636_103+232637delinsAT
XM_017005880.2:c.103+232636_103+232637delinsAT	XP_016861369.1:n.103+232636_103+232637delinsAT
XM_017005881.2:c.103+232636_103+232637delinsAT	XP_016861370.1:n.103+232636_103+232637delinsAT
XM_017005882.2:c.103+232636_103+232637delinsAT	XP_016861371.1:n.103+232636_103+232637delinsAT
XM_017005883.1:c.103+232636_103+232637delinsAT	XP_016861372.1:n.103+232636_103+232637delinsAT
XM_017005884.1:c.103+232636_103+232637delinsAT	XP_016861373.1:n.103+232636_103+232637delinsAT
NM_002012.4:c.103+232636_103+232637delinsAT MANE Select	NP_002003.1:n.103+232636_103+232637delinsAT
NM_001166243.3:c.103+232636_103+232637delinsAT	NP_001159715.1:n.103+232636_103+232637delinsAT
NM_001320899.2:c.103+232636_103+232637delinsAT	NP_001307828.1:n.103+232636_103+232637delinsAT
NM_001320900.2:c.103+232636_103+232637delinsAT	NP_001307829.1:n.103+232636_103+232637delinsAT
NM_001354589.2:c.103+232636_103+232637delinsAT	NP_001341518.1:n.103+232636_103+232637delinsAT
NM_001354590.2:c.103+232636_103+232637delinsAT	NP_001341519.1:n.103+232636_103+232637delinsAT