Canonical Allele Identifier: CA1619031009

Gene: TCF19

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161850G= , CM000668.2:g.31161850G=	GRCh38
NC_000006.11:g.31129627G= , CM000668.1:g.31129627G=	GRCh37
NC_000006.10:g.31237606G=	NCBI36
NG_054878.1:g.1389C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.642G=	ENSP00000439397.2:p.Thr214=
ENST00000706778.1:c.642G=	ENSP00000516543.1:p.Thr214=
ENST00000706779.1:c.642G=	ENSP00000516544.1:p.Thr214=
ENST00000706780.1:c.642G=	ENSP00000516545.1:p.Thr214=
ENST00000706781.1:c.642G=	ENSP00000516546.1:p.Thr214=
ENST00000706782.1:c.642G=	ENSP00000516547.1:p.Thr214=
ENST00000706783.1:c.473G=	ENSP00000516548.1:p.Arg158=
ENST00000706785.1:c.427G=	ENSP00000516549.1:p.Ala143=
ENST00000706786.1:c.473G=	ENSP00000516550.1:p.Arg158=
ENST00000706787.1:c.642G=	ENSP00000516551.1:p.Thr214=
ENST00000706788.1:n.593G=
ENST00000376257.8:c.642G= MANE Select	ENSP00000365433.3:p.Thr214=
ENST00000376255.4:c.642G=	ENSP00000365431.4:p.Thr214=
ENST00000376257.7:c.642G=	ENSP00000365433.3:p.Thr214=
ENST00000496421.1:n.194G=
ENST00000542218.1:c.402G=	ENSP00000439397.1:p.Thr134=
NM_001077511.1:c.642G=	NP_001070979.1:p.Thr214=
NM_007109.2:c.642G=	NP_009040.2:p.Thr214=
XM_005249334.2:c.642G=	XP_005249391.1:p.Thr214=
XM_011514829.1:c.642G=	XP_011513131.1:p.Thr214=
NM_001318908.1:c.642G=	NP_001305837.1:p.Thr214=
NM_007109.3:c.642G= MANE Select	NP_009040.2:p.Thr214=
NM_001077511.2:c.642G=	NP_001070979.1:p.Thr214=
NM_001318908.2:c.642G=	NP_001305837.1:p.Thr214=