Canonical Allele Identifier: CA15270835
Gene: FHIT HGNC NCBI

Linked Data

dbSNP Id: rs11919041

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.60777523G>T , CM000665.2:g.60777523G>T GRCh38
NC_000003.11:g.60763256G>T , CM000665.1:g.60763256G>T GRCh37
NC_000003.10:g.60738296G>T NCBI36
NG_007551.1:g.478878C>A
NG_007551.2:g.478937C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000492590.6:c.-18+44396C>A MANE Select ENSP00000418582.1:p.=
ENST00000468189.5:c.-18+44396C>A ENSP00000417480.1:p.=
ENST00000476844.5:c.-18+44396C>A ENSP00000417557.1:p.=
ENST00000488467.5:c.-57-11960C>A ENSP00000418596.1:p.=
ENST00000490952.1:n.550+44396C>A
ENST00000492590.5:c.-18+44396C>A ENSP00000418582.1:p.=
NM_001166243.1:c.-18+44396C>A NP_001159715.1:p.=
NM_002012.2:c.-18+44396C>A NP_002003.1:p.=
XM_011533481.1:c.-90+44396C>A XP_011531783.1:p.=
XM_011533482.1:c.-143-10425C>A XP_011531784.1:p.=
XM_011533483.1:c.-215-10425C>A XP_011531785.1:p.=
XM_011533484.1:c.-57-11960C>A XP_011531786.1:p.=
NM_001166243.2:c.-18+44396C>A NP_001159715.1:p.=
NM_001320899.1:c.-18+44396C>A NP_001307828.1:p.=
NM_001320900.1:c.-18+44396C>A NP_001307829.1:p.=
NM_001354589.1:c.-18+44396C>A NP_001341518.1:p.=
NM_001354590.1:c.-18+44396C>A NP_001341519.1:p.=
NM_002012.3:c.-18+44396C>A NP_002003.1:p.=
NR_148921.1:n.356+44396C>A
XM_017005880.2:c.-18+44396C>A XP_016861369.1:p.=
XM_017005881.2:c.-18+44396C>A XP_016861370.1:p.=
XM_017005882.2:c.-18+44396C>A XP_016861371.1:p.=
XM_017005883.1:c.-18+44396C>A XP_016861372.1:p.=
XM_017005884.1:c.-18+44396C>A XP_016861373.1:p.=
NM_002012.4:c.-18+44396C>A MANE Select NP_002003.1:p.=
NM_001166243.3:c.-18+44396C>A NP_001159715.1:p.=
NM_001320899.2:c.-18+44396C>A NP_001307828.1:p.=
NM_001320900.2:c.-18+44396C>A NP_001307829.1:p.=
NM_001354589.2:c.-18+44396C>A NP_001341518.1:p.=
NM_001354590.2:c.-18+44396C>A NP_001341519.1:p.=
NR_148921.2:n.347+44396C>A