Canonical Allele Identifier: CA1583932603

Gene: TCF7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134143082G= , CM000667.2:g.134143082G=	GRCh38
NC_000005.9:g.133478773G= , CM000667.1:g.133478773G=	GRCh37
NC_000005.8:g.133506672G=	NCBI36
NG_030367.1:g.33372G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003202.5:c.1008G= MANE Select	NP_003193.2:p.Trp336=
ENST00000342854.10:c.1008G= MANE Select	ENSP00000340347.5:p.Trp336=
NM_001134851.2:c.663G=	NP_001128323.2:p.Trp221=
NM_001134851.3:c.663G=	NP_001128323.2:p.Trp221=
NM_001134851.4:c.663G=	NP_001128323.2:p.Trp221=
NM_001346425.1:c.1101G=	NP_001333354.1:p.Trp367=
NM_001346425.2:c.1101G=	NP_001333354.1:p.Trp367=
NM_001346450.1:c.756G=	NP_001333379.1:p.Trp252=
NM_001346450.2:c.756G=	NP_001333379.1:p.Trp252=
NM_001366502.1:c.588G=	NP_001353431.1:p.Trp196=
NM_001366502.2:c.588G=	NP_001353431.1:p.Trp196=
NM_003202.3:c.1008G=	NP_003193.2:p.Trp336=
NM_003202.4:c.1008G=	NP_003193.2:p.Trp336=
NM_201632.3:c.663G=	NP_963963.1:p.Trp221=
NM_201632.4:c.663G=	NP_963963.1:p.Trp221=
NM_201632.5:c.663G=	NP_963963.1:p.Trp221=
NM_201634.3:c.663G=	NP_963965.1:p.Trp221=
NM_201634.4:c.663G=	NP_963965.1:p.Trp221=
NM_201634.5:c.663G=	NP_963965.1:p.Trp221=
NM_213648.3:c.663G=	NP_998813.1:p.Trp221=
NM_213648.4:c.663G=	NP_998813.1:p.Trp221=
NM_213648.5:c.663G=	NP_998813.1:p.Trp221=
NR_033449.1:n.995G=
NR_033449.2:n.1091G=
NR_033449.3:n.1041G=
ENST00000342854.9:c.1008G=	ENSP00000340347.5:p.Trp336=
ENST00000378560.8:c.663G=	ENSP00000367822.4:p.Trp221=
ENST00000395023.5:c.663G=	ENSP00000378469.1:p.Trp221=
ENST00000395029.5:c.1008G=	ENSP00000378472.1:p.Trp336=
ENST00000517799.5:c.342G=	ENSP00000427968.1:p.Trp114=
ENST00000517855.5:c.373G=
ENST00000518915.5:c.663G=	ENSP00000430179.1:p.Trp221=
ENST00000519238.1:n.1094G=
ENST00000520699.1:c.182G=
ENST00000520958.5:c.663G=	ENSP00000429547.1:p.Trp221=
ENST00000522375.6:c.756G=	ENSP00000427870.2:p.Trp252=
ENST00000522653.5:n.930G=
ENST00000524342.5:n.836G=
XM_006714678.2:c.1101G=	XP_006714741.1:p.Trp367=
XM_006714678.3:c.1101G=	XP_006714741.1:p.Trp367=
XM_006714679.2:c.1008G=	XP_006714742.1:p.Trp336=
XM_006714679.3:c.1008G=	XP_006714742.1:p.Trp336=
XM_006714680.2:c.1101G=	XP_006714743.1:p.Trp367=
XM_006714682.2:c.1101G=	XP_006714745.1:p.Trp367=
XM_006714684.2:c.1008G=	XP_006714747.1:p.Trp336=
XM_006714685.2:c.756G=	XP_006714748.1:p.Trp252=
XM_006714685.4:c.756G=	XP_006714748.1:p.Trp252=
XM_006714686.2:c.663G=	XP_006714749.1:p.Trp221=
XM_006714686.4:c.663G=	XP_006714749.1:p.Trp221=
XM_006714687.2:c.495G=	XP_006714750.1:p.Trp165=
XM_011543604.1:c.1101G=	XP_011541906.1:p.Trp367=
XM_011543604.2:c.1101G=	XP_011541906.1:p.Trp367=
XM_011543605.1:c.1101G=	XP_011541907.1:p.Trp367=
XM_011543606.1:c.1101G=	XP_011541908.1:p.Trp367=
XM_011543607.1:c.744G=	XP_011541909.1:p.Trp248=
XM_011543607.2:c.744G=	XP_011541909.1:p.Trp248=
XM_011543608.1:c.681G=	XP_011541910.1:p.Trp227=
XM_011543608.2:c.681G=	XP_011541910.1:p.Trp227=
XM_011543609.1:c.588G=	XP_011541911.1:p.Trp196=
XM_011543609.2:c.588G=	XP_011541911.1:p.Trp196=
XM_011543610.1:c.495G=	XP_011541912.1:p.Trp165=
XM_011543611.1:c.495G=	XP_011541913.1:p.Trp165=
XM_011543612.1:c.588G=	XP_011541914.1:p.Trp196=
XM_011543613.1:c.402G=	XP_011541915.1:p.Trp134=
XM_011543613.3:c.402G=	XP_011541915.1:p.Trp134=
XM_017009790.1:c.495G=	XP_016865279.1:p.Trp165=
XR_948292.1:n.1265G=
XR_948293.1:n.1265G=