Canonical Allele Identifier: CA504902644

Gene: TCF3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1615301C>T , CM000681.2:g.1615301C>T	GRCh38
NC_000019.9:g.1615300C>T , CM000681.1:g.1615300C>T	GRCh37
NC_000019.8:g.1566300C>T	NCBI36
NG_029953.1:g.42029G>A
NG_029953.2:g.42246G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000705032.1:c.*1544G>A	ENSP00000516067.1:n.*1544G>A
ENST00000262965.12:c.1806G>A MANE Select	ENSP00000262965.5:p.Leu602=
ENST00000588136.7:c.1586+385G>A MANE Plus Clinical	ENSP00000468487.1:n.1586+385G>A
ENST00000611869.5:c.1586+385G>A	ENSP00000480564.2:n.1586+385G>A
ENST00000651991.1:c.362G>A
ENST00000262965.9:c.1806G>A	ENSP00000262965.4:p.Leu602=
ENST00000344749.9:c.1433+385G>A	ENSP00000344375.6:n.1433+385G>A
ENST00000395423.7:c.1818G>A	ENSP00000378813.3:p.Leu606=
ENST00000453954.6:c.1673+385G>A	ENSP00000396363.3:n.1673+385G>A
ENST00000585731.5:c.113+385G>A	ENSP00000465510.2:n.113+385G>A
ENST00000585855.2:c.391G>A	ENSP00000465481.1:n.391G>A
ENST00000586164.1:c.298G>A	ENSP00000467972.1:n.298G>A
ENST00000587425.5:c.339G>A	ENSP00000467508.2:p.Leu113=
ENST00000588136.5:c.1586+385G>A	ENSP00000468487.1:n.1586+385G>A
ENST00000590436.5:c.574+385G>A
ENST00000590684.5:c.292+385G>A
ENST00000592395.5:c.298G>A	ENSP00000465251.1:n.298G>A
ENST00000592628.5:c.381G>A	ENSP00000465549.1:p.Leu127=
ENST00000593064.5:c.455G>A
ENST00000610756.4:n.1164G>A
ENST00000611869.4:c.1806G>A	ENSP00000480564.1:p.Leu602=
NM_001136139.2:c.1586+385G>A	NP_001129611.1:n.1586+385G>A
NM_003200.3:c.1806G>A	NP_003191.1:p.Leu602=
XM_006722852.2:c.1893G>A	XP_006722915.1:p.Leu631=
XM_006722853.2:c.1893G>A	XP_006722916.1:p.Leu631=
XM_006722855.2:c.1673+385G>A	XP_006722918.1:n.1673+385G>A
XM_006722856.2:c.1673+385G>A	XP_006722919.1:n.1673+385G>A
XM_006722857.2:c.1673+385G>A	XP_006722920.1:n.1673+385G>A
XM_006722858.2:c.1673+385G>A	XP_006722921.1:n.1673+385G>A
XM_011528215.1:c.1893G>A	XP_011526517.1:p.Leu631=
XM_011528216.1:c.1893G>A	XP_011526518.1:p.Leu631=
XM_011528217.1:c.1893G>A	XP_011526519.1:p.Leu631=
XM_011528218.1:c.1893G>A	XP_011526520.1:p.Leu631=
XM_011528219.1:c.1890G>A	XP_011526521.1:p.Leu630=
XM_011528220.1:c.1673+385G>A	XP_011526522.1:n.1673+385G>A
XM_011528221.1:c.1673+385G>A	XP_011526523.1:n.1673+385G>A
XM_011528222.1:c.1818G>A	XP_011526524.1:p.Leu606=
XM_011528223.1:c.1803G>A	XP_011526525.1:p.Leu601=
XM_011528224.1:c.1586+385G>A	XP_011526526.1:n.1586+385G>A
XM_011528225.1:c.1586+385G>A	XP_011526527.1:n.1586+385G>A
XM_011528226.1:c.1583+385G>A	XP_011526528.1:n.1583+385G>A
XM_011528227.1:c.1433+385G>A	XP_011526529.1:n.1433+385G>A
XR_430150.2:n.3319G>A
XR_430151.2:n.3319G>A
XR_430152.2:n.3287G>A
XR_430153.2:n.3287G>A
NM_001136139.3:c.1586+385G>A	NP_001129611.1:n.1586+385G>A
NM_001351778.1:c.1803G>A	NP_001338707.1:p.Leu601=
NM_001351779.1:c.1586+385G>A	NP_001338708.1:n.1586+385G>A
NM_003200.4:c.1806G>A	NP_003191.1:p.Leu602=
XM_006722855.4:c.1673+385G>A	XP_006722918.1:n.1673+385G>A
XM_006722857.4:c.1673+385G>A	XP_006722920.1:n.1673+385G>A
XM_006722858.3:c.1673+385G>A	XP_006722921.1:n.1673+385G>A
XM_011528216.2:c.1893G>A	XP_011526518.1:p.Leu631=
XM_011528219.2:c.1890G>A	XP_011526521.1:p.Leu630=
XM_011528220.2:c.1673+385G>A	XP_011526522.1:n.1673+385G>A
XM_011528221.2:c.1673+385G>A	XP_011526523.1:n.1673+385G>A
XM_011528223.3:c.1803G>A	XP_011526525.1:p.Leu601=
XM_011528225.2:c.1586+385G>A	XP_011526527.1:n.1586+385G>A
XM_011528226.2:c.1583+385G>A	XP_011526528.1:n.1583+385G>A
XM_011528227.3:c.1433+385G>A	XP_011526529.1:n.1433+385G>A
XM_017027177.2:c.1893G>A	XP_016882666.1:p.Leu631=
XM_017027178.1:c.1673+385G>A	XP_016882667.1:n.1673+385G>A
XM_017027179.2:c.1670+385G>A	XP_016882668.1:n.1670+385G>A
XM_017027180.2:c.1818G>A	XP_016882669.1:p.Leu606=
XM_017027181.1:c.1806G>A	XP_016882670.1:p.Leu602=
XM_017027182.1:c.1586+385G>A	XP_016882671.1:n.1586+385G>A
XM_024451669.1:c.1974G>A	XP_024307437.1:p.Leu658=
XM_024451670.1:c.1974G>A	XP_024307438.1:p.Leu658=
XM_024451671.1:c.1974G>A	XP_024307439.1:p.Leu658=
XM_024451672.1:c.1974G>A	XP_024307440.1:p.Leu658=
XM_024451673.1:c.1974G>A	XP_024307441.1:p.Leu658=
XM_024451674.1:c.1974G>A	XP_024307442.1:p.Leu658=
XM_024451675.1:c.1754+385G>A	XP_024307443.1:n.1754+385G>A
XM_024451676.1:c.1754+385G>A	XP_024307444.1:n.1754+385G>A
XM_024451677.1:c.1754+385G>A	XP_024307445.1:n.1754+385G>A
XM_024451678.1:c.1754+385G>A	XP_024307446.1:n.1754+385G>A
XM_024451679.1:c.1887G>A	XP_024307447.1:p.Leu629=
XM_024451680.1:c.1974G>A	XP_024307448.1:p.Leu658=
XR_001753743.2:n.2053G>A
XR_001753745.1:n.2051G>A
XR_001753747.1:n.2019G>A
XR_002958346.1:n.2135G>A
XR_002958347.1:n.2135G>A
XR_002958348.1:n.2136G>A
XR_002958349.1:n.2102G>A
XR_002958350.1:n.2102G>A
XR_002958351.1:n.2102G>A
NM_001136139.4:c.1586+385G>A MANE Plus Clinical	NP_001129611.1:n.1586+385G>A
NM_003200.5:c.1806G>A MANE Select	NP_003191.1:p.Leu602=
NM_001351778.2:c.1803G>A	NP_001338707.1:p.Leu601=
NM_001351779.2:c.1586+385G>A	NP_001338708.1:n.1586+385G>A