Canonical Allele Identifier: CA353852921
Community Standard Title: NM_006070.6(TFG):c.878A>C (p.Gln293Pro)
Gene: TFG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.100748206A>C , CM000665.2:g.100748206A>C GRCh38
NC_000003.11:g.100467050A>C , CM000665.1:g.100467050A>C GRCh37
NC_000003.10:g.101949740A>C NCBI36
NG_027821.1:g.43917A>C
NG_027821.2:g.43917A>C

Transcript Alleles

HGVS Amino-acid Change
NM_006070.6:c.878A>C MANE Select NP_006061.2:p.Gln293Pro
ENST00000240851.9:c.878A>C MANE Select ENSP00000240851.4:p.Gln293Pro
NM_001007565.2:c.878A>C NP_001007566.1:p.Gln293Pro
NM_001195478.1:c.878A>C NP_001182407.1:p.Gln293Pro
NM_001195478.2:c.878A>C NP_001182407.1:p.Gln293Pro
NM_001195479.1:c.866A>C NP_001182408.1:p.Gln289Pro
NM_001195479.2:c.866A>C NP_001182408.1:p.Gln289Pro
NM_006070.5:c.878A>C NP_006061.2:p.Gln293Pro
ENST00000240851.8:c.878A>C ENSP00000240851.4:p.Gln293Pro
ENST00000418917.6:c.866A>C ENSP00000397182.2:p.Gln289Pro
ENST00000418917.7:c.*48A>C ENSP00000397182.3:n.*48A>C
ENST00000463568.6:c.866A>C ENSP00000419504.2:p.Gln289Pro
ENST00000476228.5:c.866A>C ENSP00000417952.1:p.Gln289Pro
ENST00000481203.1:n.2514A>C
ENST00000487505.6:c.878A>C ENSP00000420797.2:p.Gln293Pro
ENST00000490574.5:c.878A>C ENSP00000419960.1:p.Gln293Pro
ENST00000490574.6:c.878A>C ENSP00000419960.1:p.Gln293Pro
ENST00000612059.4:c.865A>C ENSP00000477562.1:p.Ser289Arg
ENST00000615993.1:c.919A>C ENSP00000479269.1:n.919A>C
ENST00000615993.2:c.*64A>C ENSP00000479269.2:n.*64A>C
ENST00000620299.5:c.*64A>C ENSP00000479981.1:n.*64A>C
ENST00000674615.1:c.878A>C ENSP00000502734.1:p.Gln293Pro
ENST00000674645.1:c.866A>C ENSP00000501892.1:p.Gln289Pro
ENST00000674699.1:c.*135A>C ENSP00000502175.1:n.*135A>C
ENST00000674758.1:c.866A>C ENSP00000502502.1:p.Gln289Pro
ENST00000674798.1:n.3725A>C
ENST00000675011.1:c.*173A>C ENSP00000501745.1:n.*173A>C
ENST00000675047.1:c.866A>C ENSP00000502497.1:p.Gln289Pro
ENST00000675243.1:c.878A>C ENSP00000502592.1:p.Gln293Pro
ENST00000675246.1:c.874A>C ENSP00000501620.1:p.Ser292Arg
ENST00000675420.1:c.866A>C ENSP00000502516.1:p.Gln289Pro
ENST00000675499.1:c.878A>C ENSP00000502450.1:p.Gln293Pro
ENST00000675543.1:c.*64A>C ENSP00000502229.1:n.*64A>C
ENST00000675553.1:c.878A>C ENSP00000501815.1:p.Gln293Pro
ENST00000675586.1:c.*64A>C ENSP00000502329.1:n.*64A>C
ENST00000675591.1:c.*435A>C ENSP00000501641.1:n.*435A>C
ENST00000675692.1:c.914A>C ENSP00000502034.1:p.Gln305Pro
ENST00000675890.1:c.*48A>C ENSP00000502537.1:n.*48A>C
ENST00000675958.1:c.*48A>C ENSP00000502025.1:n.*48A>C
ENST00000676010.1:n.5106A>C
ENST00000676054.1:c.*135A>C ENSP00000502051.1:n.*135A>C
ENST00000676111.1:c.*64A>C ENSP00000502139.1:n.*64A>C
ENST00000676276.1:c.*112A>C ENSP00000502372.1:n.*112A>C
ENST00000676308.1:c.*64A>C ENSP00000502697.1:n.*64A>C
ENST00000676395.1:c.878A>C ENSP00000502071.1:p.Gln293Pro
ENST00000676431.1:c.866A>C ENSP00000502698.1:p.Gln289Pro
XM_005247066.1:c.866A>C XP_005247123.1:p.Gln289Pro
XM_005247066.2:c.866A>C XP_005247123.1:p.Gln289Pro
XM_006713472.1:c.878A>C XP_006713535.1:p.Gln293Pro
XM_006713473.1:c.878A>C XP_006713536.1:p.Gln293Pro
XM_011512334.1:c.878A>C XP_011510636.1:p.Gln293Pro
XM_017005527.1:c.866A>C XP_016861016.1:p.Gln289Pro