Canonical Allele Identifier: CA1619031007

Gene: TCF19

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161847C= , CM000668.2:g.31161847C=	GRCh38
NC_000006.11:g.31129624C= , CM000668.1:g.31129624C=	GRCh37
NC_000006.10:g.31237603C=	NCBI36
NG_054878.1:g.1392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.639C=	ENSP00000439397.2:p.Thr213=
ENST00000706778.1:c.639C=	ENSP00000516543.1:p.Thr213=
ENST00000706779.1:c.639C=	ENSP00000516544.1:p.Thr213=
ENST00000706780.1:c.639C=	ENSP00000516545.1:p.Thr213=
ENST00000706781.1:c.639C=	ENSP00000516546.1:p.Thr213=
ENST00000706782.1:c.639C=	ENSP00000516547.1:p.Thr213=
ENST00000706783.1:c.470C=	ENSP00000516548.1:p.Pro157=
ENST00000706785.1:c.424C=	ENSP00000516549.1:p.His142=
ENST00000706786.1:c.470C=	ENSP00000516550.1:p.Pro157=
ENST00000706787.1:c.639C=	ENSP00000516551.1:p.Thr213=
ENST00000706788.1:n.590C=
ENST00000376257.8:c.639C= MANE Select	ENSP00000365433.3:p.Thr213=
ENST00000376255.4:c.639C=	ENSP00000365431.4:p.Thr213=
ENST00000376257.7:c.639C=	ENSP00000365433.3:p.Thr213=
ENST00000496421.1:n.191C=
ENST00000542218.1:c.399C=	ENSP00000439397.1:p.Thr133=
NM_001077511.1:c.639C=	NP_001070979.1:p.Thr213=
NM_007109.2:c.639C=	NP_009040.2:p.Thr213=
XM_005249334.2:c.639C=	XP_005249391.1:p.Thr213=
XM_011514829.1:c.639C=	XP_011513131.1:p.Thr213=
NM_001318908.1:c.639C=	NP_001305837.1:p.Thr213=
NM_007109.3:c.639C= MANE Select	NP_009040.2:p.Thr213=
NM_001077511.2:c.639C=	NP_001070979.1:p.Thr213=
NM_001318908.2:c.639C=	NP_001305837.1:p.Thr213=