Canonical Allele Identifier: CA1368590708
Gene: FHIT HGNC NCBI

Linked Data

dbSNP Id: rs1708569272

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.60304195A>C , CM000665.2:g.60304195A>C GRCh38
NC_000003.11:g.60289924A>C , CM000665.1:g.60289924A>C GRCh37
NC_000003.10:g.60264964A>C NCBI36
NG_007551.1:g.952210T>G
NG_007551.2:g.952265T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000492590.6:c.103+232665T>G MANE Select ENSP00000418582.1:n.103+232665T>G
ENST00000468189.5:c.103+232665T>G ENSP00000417480.1:n.103+232665T>G
ENST00000476844.5:c.103+232665T>G ENSP00000417557.1:n.103+232665T>G
ENST00000488467.5:c.103+232665T>G ENSP00000418596.1:n.103+232665T>G
ENST00000492590.5:c.103+232665T>G ENSP00000418582.1:n.103+232665T>G
NM_001166243.1:c.103+232665T>G NP_001159715.1:n.103+232665T>G
NM_002012.2:c.103+232665T>G NP_002003.1:n.103+232665T>G
XM_011533481.1:c.103+232665T>G XP_011531783.1:n.103+232665T>G
XM_011533482.1:c.103+232665T>G XP_011531784.1:n.103+232665T>G
XM_011533483.1:c.103+232665T>G XP_011531785.1:n.103+232665T>G
XM_011533484.1:c.103+232665T>G XP_011531786.1:n.103+232665T>G
XM_011533485.1:c.103+232665T>G XP_011531787.1:n.103+232665T>G
XM_011533486.1:c.103+232665T>G XP_011531788.1:n.103+232665T>G
NM_001166243.2:c.103+232665T>G NP_001159715.1:n.103+232665T>G
NM_001320899.1:c.103+232665T>G NP_001307828.1:n.103+232665T>G
NM_001320900.1:c.103+232665T>G NP_001307829.1:n.103+232665T>G
NM_001354589.1:c.103+232665T>G NP_001341518.1:n.103+232665T>G
NM_001354590.1:c.103+232665T>G NP_001341519.1:n.103+232665T>G
NM_002012.3:c.103+232665T>G NP_002003.1:n.103+232665T>G
XM_017005880.2:c.103+232665T>G XP_016861369.1:n.103+232665T>G
XM_017005881.2:c.103+232665T>G XP_016861370.1:n.103+232665T>G
XM_017005882.2:c.103+232665T>G XP_016861371.1:n.103+232665T>G
XM_017005883.1:c.103+232665T>G XP_016861372.1:n.103+232665T>G
XM_017005884.1:c.103+232665T>G XP_016861373.1:n.103+232665T>G
NM_002012.4:c.103+232665T>G MANE Select NP_002003.1:n.103+232665T>G
NM_001166243.3:c.103+232665T>G NP_001159715.1:n.103+232665T>G
NM_001320899.2:c.103+232665T>G NP_001307828.1:n.103+232665T>G
NM_001320900.2:c.103+232665T>G NP_001307829.1:n.103+232665T>G
NM_001354589.2:c.103+232665T>G NP_001341518.1:n.103+232665T>G
NM_001354590.2:c.103+232665T>G NP_001341519.1:n.103+232665T>G