Canonical Allele Identifier: CA3411974

Gene: TCF7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134115992C>A , CM000667.2:g.134115992C>A	GRCh38
NC_000005.9:g.133451683C>A , CM000667.1:g.133451683C>A	GRCh37
NC_000005.8:g.133479582C>A	NCBI36
NG_030367.1:g.6282C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000522375.6:c.55C>A	ENSP00000427870.2:p.Pro19Thr
ENST00000342854.10:c.400C>A MANE Select	ENSP00000340347.5:p.Pro134Thr
ENST00000342854.9:c.400C>A	ENSP00000340347.5:p.Pro134Thr
ENST00000378560.8:c.55C>A	ENSP00000367822.4:p.Pro19Thr
ENST00000395023.5:c.55C>A	ENSP00000378469.1:p.Pro19Thr
ENST00000395029.5:c.400C>A	ENSP00000378472.1:p.Pro134Thr
ENST00000517741.5:c.55C>A	ENSP00000427758.1:p.Pro19Thr
ENST00000517851.5:c.55C>A	ENSP00000429946.1:p.Pro19Thr
ENST00000518887.5:c.55C>A	ENSP00000430617.1:p.Pro19Thr
ENST00000518915.5:c.55C>A	ENSP00000430179.1:p.Pro19Thr
ENST00000519165.1:n.82C>A
ENST00000519447.5:c.55C>A	ENSP00000431095.1:p.Pro19Thr
ENST00000520652.5:c.37C>A	ENSP00000429817.1:p.Pro13Thr
ENST00000520958.5:c.55C>A	ENSP00000429547.1:p.Pro19Thr
ENST00000521639.5:c.55C>A	ENSP00000427782.1:p.Pro19Thr
ENST00000522375.5:c.55C>A	ENSP00000427870.1:p.Pro19Thr
ENST00000522653.5:n.120C>A
NM_001134851.2:c.55C>A	NP_001128323.2:p.Pro19Thr
NM_003202.3:c.400C>A	NP_003193.2:p.Pro134Thr
NM_201632.3:c.55C>A	NP_963963.1:p.Pro19Thr
NM_201634.3:c.55C>A	NP_963965.1:p.Pro19Thr
NM_213648.3:c.55C>A	NP_998813.1:p.Pro19Thr
NR_033449.1:n.334C>A
XM_006714678.2:c.400C>A	XP_006714741.1:p.Pro134Thr
XM_006714679.2:c.400C>A	XP_006714742.1:p.Pro134Thr
XM_006714680.2:c.400C>A	XP_006714743.1:p.Pro134Thr
XM_006714682.2:c.400C>A	XP_006714745.1:p.Pro134Thr
XM_006714684.2:c.400C>A	XP_006714747.1:p.Pro134Thr
XM_006714685.2:c.55C>A	XP_006714748.1:p.Pro19Thr
XM_006714686.2:c.55C>A	XP_006714749.1:p.Pro19Thr
XM_011543604.1:c.400C>A	XP_011541906.1:p.Pro134Thr
XM_011543605.1:c.400C>A	XP_011541907.1:p.Pro134Thr
XM_011543606.1:c.400C>A	XP_011541908.1:p.Pro134Thr
XM_011543610.1:c.-260C>A	XP_011541912.1:n.-260C>A
XM_011543613.1:c.-260C>A	XP_011541915.1:n.-260C>A
XR_948292.1:n.604C>A
XR_948293.1:n.604C>A
XR_948294.1:n.604C>A
NM_001134851.3:c.55C>A	NP_001128323.2:p.Pro19Thr
NM_001346425.1:c.400C>A	NP_001333354.1:p.Pro134Thr
NM_001346450.1:c.55C>A	NP_001333379.1:p.Pro19Thr
NM_003202.4:c.400C>A	NP_003193.2:p.Pro134Thr
NM_201632.4:c.55C>A	NP_963963.1:p.Pro19Thr
NM_201634.4:c.55C>A	NP_963965.1:p.Pro19Thr
NM_213648.4:c.55C>A	NP_998813.1:p.Pro19Thr
NR_033449.2:n.430C>A
XM_006714678.3:c.400C>A	XP_006714741.1:p.Pro134Thr
XM_006714679.3:c.400C>A	XP_006714742.1:p.Pro134Thr
XM_006714685.4:c.55C>A	XP_006714748.1:p.Pro19Thr
XM_006714686.4:c.55C>A	XP_006714749.1:p.Pro19Thr
XM_011543604.2:c.400C>A	XP_011541906.1:p.Pro134Thr
XM_011543613.3:c.-260C>A	XP_011541915.1:n.-260C>A
XR_001742231.1:n.604C>A
XR_001742232.1:n.604C>A
XR_948294.2:n.604C>A
NM_003202.5:c.400C>A MANE Select	NP_003193.2:p.Pro134Thr
NM_001134851.4:c.55C>A	NP_001128323.2:p.Pro19Thr
NM_001346425.2:c.400C>A	NP_001333354.1:p.Pro134Thr
NM_001346450.2:c.55C>A	NP_001333379.1:p.Pro19Thr
NM_201632.5:c.55C>A	NP_963963.1:p.Pro19Thr
NM_201634.5:c.55C>A	NP_963965.1:p.Pro19Thr
NM_213648.5:c.55C>A	NP_998813.1:p.Pro19Thr
NR_033449.3:n.380C>A