Canonical Allele Identifier: CA2517084

Gene: TFG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.100732499T>C , CM000665.2:g.100732499T>C	GRCh38
NC_000003.11:g.100451343T>C , CM000665.1:g.100451343T>C	GRCh37
NC_000003.10:g.101934033T>C	NCBI36
NG_027821.1:g.28210T>C
NG_027821.2:g.28210T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000240851.9:c.416-9T>C MANE Select	ENSP00000240851.4:n.416-9T>C
ENST00000418917.7:c.416-9T>C	ENSP00000397182.3:n.416-9T>C
ENST00000463568.6:c.416-9T>C	ENSP00000419504.2:n.416-9T>C
ENST00000487505.6:c.416-9T>C	ENSP00000420797.2:n.416-9T>C
ENST00000490574.6:c.416-9T>C	ENSP00000419960.1:n.416-9T>C
ENST00000615993.2:c.416-9T>C	ENSP00000479269.2:n.416-9T>C
ENST00000620299.5:c.416-9T>C	ENSP00000479981.1:n.416-9T>C
ENST00000674615.1:c.416-9T>C	ENSP00000502734.1:n.416-9T>C
ENST00000674645.1:c.416-9T>C	ENSP00000501892.1:n.416-9T>C
ENST00000674699.1:c.416-9T>C	ENSP00000502175.1:n.416-9T>C
ENST00000674758.1:c.416-9T>C	ENSP00000502502.1:n.416-9T>C
ENST00000674798.1:n.752-9T>C
ENST00000675011.1:c.416-9T>C	ENSP00000501745.1:n.416-9T>C
ENST00000675047.1:c.416-9T>C	ENSP00000502497.1:n.416-9T>C
ENST00000675243.1:c.416-9T>C	ENSP00000502592.1:n.416-9T>C
ENST00000675246.1:c.416-9T>C	ENSP00000501620.1:n.416-9T>C
ENST00000675420.1:c.416-9T>C	ENSP00000502516.1:n.416-9T>C
ENST00000675499.1:c.416-9T>C	ENSP00000502450.1:n.416-9T>C
ENST00000675543.1:c.416-9T>C	ENSP00000502229.1:n.416-9T>C
ENST00000675553.1:c.416-9T>C	ENSP00000501815.1:n.416-9T>C
ENST00000675586.1:c.416-9T>C	ENSP00000502329.1:n.416-9T>C
ENST00000675591.1:c.570-9T>C	ENSP00000501641.1:n.570-9T>C
ENST00000675692.1:c.416-9T>C	ENSP00000502034.1:n.416-9T>C
ENST00000675890.1:c.416-9T>C	ENSP00000502537.1:n.416-9T>C
ENST00000675958.1:c.416-9T>C	ENSP00000502025.1:n.416-9T>C
ENST00000676010.1:n.741-9T>C
ENST00000676054.1:c.416-9T>C	ENSP00000502051.1:n.416-9T>C
ENST00000676111.1:c.416-9T>C	ENSP00000502139.1:n.416-9T>C
ENST00000676276.1:c.416-9T>C	ENSP00000502372.1:n.416-9T>C
ENST00000676308.1:c.416-9T>C	ENSP00000502697.1:n.416-9T>C
ENST00000676395.1:c.416-9T>C	ENSP00000502071.1:n.416-9T>C
ENST00000676431.1:c.416-9T>C	ENSP00000502698.1:n.416-9T>C
ENST00000676455.1:c.416-9T>C	ENSP00000502625.1:n.416-9T>C
ENST00000240851.8:c.416-9T>C	ENSP00000240851.4:n.416-9T>C
ENST00000418917.6:c.416-9T>C	ENSP00000397182.2:n.416-9T>C
ENST00000463568.5:c.416-9T>C	ENSP00000419504.1:n.416-9T>C
ENST00000476228.5:c.416-9T>C	ENSP00000417952.1:n.416-9T>C
ENST00000487505.5:c.416-9T>C	ENSP00000420797.1:n.416-9T>C
ENST00000490574.5:c.416-9T>C	ENSP00000419960.1:n.416-9T>C
ENST00000612059.4:c.416-9T>C	ENSP00000477562.1:n.416-9T>C
ENST00000615993.1:c.416-9T>C	ENSP00000479269.1:n.416-9T>C
ENST00000620299.4:c.416-9T>C	ENSP00000479981.1:n.416-9T>C
NM_001007565.2:c.416-9T>C	NP_001007566.1:n.416-9T>C
NM_001195478.1:c.416-9T>C	NP_001182407.1:n.416-9T>C
NM_001195479.1:c.416-9T>C	NP_001182408.1:n.416-9T>C
NM_006070.5:c.416-9T>C	NP_006061.2:n.416-9T>C
XM_005247066.1:c.416-9T>C	XP_005247123.1:n.416-9T>C
XM_006713472.1:c.416-9T>C	XP_006713535.1:n.416-9T>C
XM_006713473.1:c.416-9T>C	XP_006713536.1:n.416-9T>C
XM_011512334.1:c.416-9T>C	XP_011510636.1:n.416-9T>C
XM_005247066.2:c.416-9T>C	XP_005247123.1:n.416-9T>C
XM_017005527.1:c.416-9T>C	XP_016861016.1:n.416-9T>C
NM_006070.6:c.416-9T>C MANE Select	NP_006061.2:n.416-9T>C
NM_001195478.2:c.416-9T>C	NP_001182407.1:n.416-9T>C
NM_001195479.2:c.416-9T>C	NP_001182408.1:n.416-9T>C