Canonical Allele Identifier: CA9049648

Gene: TCF3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1615394C>T , CM000681.2:g.1615394C>T	GRCh38
NC_000019.9:g.1615393C>T , CM000681.1:g.1615393C>T	GRCh37
NC_000019.8:g.1566393C>T	NCBI36
NG_029953.1:g.41936G>A
NG_029953.2:g.42153G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003200.5:c.1713G>A MANE Select	NP_003191.1:p.Glu571=
ENST00000262965.12:c.1713G>A MANE Select	ENSP00000262965.5:p.Glu571=
NM_001136139.4:c.1586+292G>A MANE Plus Clinical	NP_001129611.1:n.1586+292G>A
ENST00000588136.7:c.1586+292G>A MANE Plus Clinical	ENSP00000468487.1:n.1586+292G>A
NM_001136139.2:c.1586+292G>A	NP_001129611.1:n.1586+292G>A
NM_001136139.3:c.1586+292G>A	NP_001129611.1:n.1586+292G>A
NM_001351778.1:c.1710G>A	NP_001338707.1:p.Glu570=
NM_001351778.2:c.1710G>A	NP_001338707.1:p.Glu570=
NM_001351779.1:c.1586+292G>A	NP_001338708.1:n.1586+292G>A
NM_001351779.2:c.1586+292G>A	NP_001338708.1:n.1586+292G>A
NM_003200.3:c.1713G>A	NP_003191.1:p.Glu571=
NM_003200.4:c.1713G>A	NP_003191.1:p.Glu571=
ENST00000262965.9:c.1713G>A	ENSP00000262965.4:p.Glu571=
ENST00000344749.9:c.1433+292G>A	ENSP00000344375.6:n.1433+292G>A
ENST00000395423.7:c.1725G>A	ENSP00000378813.3:p.Glu575=
ENST00000453954.6:c.1673+292G>A	ENSP00000396363.3:n.1673+292G>A
ENST00000585731.5:c.113+292G>A	ENSP00000465510.2:n.113+292G>A
ENST00000585855.2:c.298G>A	ENSP00000465481.1:n.298G>A
ENST00000586164.1:c.205G>A	ENSP00000467972.1:n.205G>A
ENST00000587425.5:c.246G>A	ENSP00000467508.2:p.Glu82=
ENST00000588136.5:c.1586+292G>A	ENSP00000468487.1:n.1586+292G>A
ENST00000590436.5:c.574+292G>A
ENST00000590684.5:c.292+292G>A
ENST00000592395.5:c.205G>A	ENSP00000465251.1:n.205G>A
ENST00000592628.5:c.288G>A	ENSP00000465549.1:p.Glu96=
ENST00000593064.5:c.362G>A
ENST00000610756.4:n.1071G>A
ENST00000611869.4:c.1713G>A	ENSP00000480564.1:p.Glu571=
ENST00000611869.5:c.1586+292G>A	ENSP00000480564.2:n.1586+292G>A
ENST00000651991.1:c.269G>A
ENST00000705032.1:c.*1451G>A	ENSP00000516067.1:n.*1451G>A
XM_006722852.2:c.1800G>A	XP_006722915.1:p.Glu600=
XM_006722853.2:c.1800G>A	XP_006722916.1:p.Glu600=
XM_006722855.2:c.1673+292G>A	XP_006722918.1:n.1673+292G>A
XM_006722855.4:c.1673+292G>A	XP_006722918.1:n.1673+292G>A
XM_006722856.2:c.1673+292G>A	XP_006722919.1:n.1673+292G>A
XM_006722857.2:c.1673+292G>A	XP_006722920.1:n.1673+292G>A
XM_006722857.4:c.1673+292G>A	XP_006722920.1:n.1673+292G>A
XM_006722858.2:c.1673+292G>A	XP_006722921.1:n.1673+292G>A
XM_006722858.3:c.1673+292G>A	XP_006722921.1:n.1673+292G>A
XM_011528215.1:c.1800G>A	XP_011526517.1:p.Glu600=
XM_011528216.1:c.1800G>A	XP_011526518.1:p.Glu600=
XM_011528216.2:c.1800G>A	XP_011526518.1:p.Glu600=
XM_011528217.1:c.1800G>A	XP_011526519.1:p.Glu600=
XM_011528218.1:c.1800G>A	XP_011526520.1:p.Glu600=
XM_011528219.1:c.1797G>A	XP_011526521.1:p.Glu599=
XM_011528219.2:c.1797G>A	XP_011526521.1:p.Glu599=
XM_011528220.1:c.1673+292G>A	XP_011526522.1:n.1673+292G>A
XM_011528220.2:c.1673+292G>A	XP_011526522.1:n.1673+292G>A
XM_011528221.1:c.1673+292G>A	XP_011526523.1:n.1673+292G>A
XM_011528221.2:c.1673+292G>A	XP_011526523.1:n.1673+292G>A
XM_011528222.1:c.1725G>A	XP_011526524.1:p.Glu575=
XM_011528223.1:c.1710G>A	XP_011526525.1:p.Glu570=
XM_011528223.3:c.1710G>A	XP_011526525.1:p.Glu570=
XM_011528224.1:c.1586+292G>A	XP_011526526.1:n.1586+292G>A
XM_011528225.1:c.1586+292G>A	XP_011526527.1:n.1586+292G>A
XM_011528225.2:c.1586+292G>A	XP_011526527.1:n.1586+292G>A
XM_011528226.1:c.1583+292G>A	XP_011526528.1:n.1583+292G>A
XM_011528226.2:c.1583+292G>A	XP_011526528.1:n.1583+292G>A
XM_011528227.1:c.1433+292G>A	XP_011526529.1:n.1433+292G>A
XM_011528227.3:c.1433+292G>A	XP_011526529.1:n.1433+292G>A
XM_017027177.2:c.1800G>A	XP_016882666.1:p.Glu600=
XM_017027178.1:c.1673+292G>A	XP_016882667.1:n.1673+292G>A
XM_017027179.2:c.1670+292G>A	XP_016882668.1:n.1670+292G>A
XM_017027180.2:c.1725G>A	XP_016882669.1:p.Glu575=
XM_017027181.1:c.1713G>A	XP_016882670.1:p.Glu571=
XM_017027182.1:c.1586+292G>A	XP_016882671.1:n.1586+292G>A
XM_024451669.1:c.1881G>A	XP_024307437.1:p.Glu627=
XM_024451670.1:c.1881G>A	XP_024307438.1:p.Glu627=
XM_024451671.1:c.1881G>A	XP_024307439.1:p.Glu627=
XM_024451672.1:c.1881G>A	XP_024307440.1:p.Glu627=
XM_024451673.1:c.1881G>A	XP_024307441.1:p.Glu627=
XM_024451674.1:c.1881G>A	XP_024307442.1:p.Glu627=
XM_024451675.1:c.1754+292G>A	XP_024307443.1:n.1754+292G>A
XM_024451676.1:c.1754+292G>A	XP_024307444.1:n.1754+292G>A
XM_024451677.1:c.1754+292G>A	XP_024307445.1:n.1754+292G>A
XM_024451678.1:c.1754+292G>A	XP_024307446.1:n.1754+292G>A
XM_024451679.1:c.1794G>A	XP_024307447.1:p.Glu598=
XM_024451680.1:c.1881G>A	XP_024307448.1:p.Glu627=
XR_001753743.2:n.1960G>A
XR_001753745.1:n.1958G>A
XR_001753747.1:n.1926G>A
XR_002958346.1:n.2042G>A
XR_002958347.1:n.2042G>A
XR_002958348.1:n.2043G>A
XR_002958349.1:n.2009G>A
XR_002958350.1:n.2009G>A
XR_002958351.1:n.2009G>A
XR_430150.2:n.3226G>A
XR_430151.2:n.3226G>A
XR_430152.2:n.3194G>A
XR_430153.2:n.3194G>A