Canonical Allele Identifier: CA2677940370

Gene: TCF19

Linked Data

• gnomAD v4: 6-31161840-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161843_31161844dup , CM000668.2:g.31161843_31161844dup	GRCh38
NC_000006.11:g.31129620_31129621dup , CM000668.1:g.31129620_31129621dup	GRCh37
NC_000006.10:g.31237599_31237600dup	NCBI36
NG_054878.1:g.1397_1398dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000542218.2:c.635_636dup	ENSP00000439397.2:p.Thr213GlyfsTer?
ENST00000706778.1:c.635_636dup	ENSP00000516543.1:p.Thr213GlyfsTer?
ENST00000706779.1:c.635_636dup	ENSP00000516544.1:p.Thr213GlyfsTer?
ENST00000706780.1:c.635_636dup	ENSP00000516545.1:p.Thr213GlyfsTer?
ENST00000706781.1:c.635_636dup	ENSP00000516546.1:p.Thr213GlyfsTer?
ENST00000706782.1:c.635_636dup	ENSP00000516547.1:p.Thr213GlyfsTer?
ENST00000706783.1:c.466_467dup	ENSP00000516548.1:p.Pro157AspfsTer24
ENST00000706785.1:c.420_421dup	ENSP00000516549.1:p.Asp141GlyfsTer?
ENST00000706786.1:c.466_467dup	ENSP00000516550.1:p.Pro157AspfsTer24
ENST00000706787.1:c.635_636dup	ENSP00000516551.1:p.Thr213GlyfsTer?
ENST00000706788.1:n.586_587dup
ENST00000376257.8:c.635_636dup MANE Select	ENSP00000365433.3:p.Thr213GlyfsTer?
ENST00000376255.4:c.635_636dup	ENSP00000365431.4:p.Thr213GlyfsTer?
ENST00000376257.7:c.635_636dup	ENSP00000365433.3:p.Thr213GlyfsTer?
ENST00000496421.1:n.187_188dup
ENST00000542218.1:c.395_396dup	ENSP00000439397.1:p.Thr133GlyfsTer?
NM_001077511.1:c.635_636dup	NP_001070979.1:p.Thr213GlyfsTer?
NM_007109.2:c.635_636dup	NP_009040.2:p.Thr213GlyfsTer?
XM_005249334.2:c.635_636dup	XP_005249391.1:p.Thr213GlyfsTer?
XM_011514829.1:c.635_636dup	XP_011513131.1:p.Thr213GlyfsTer?
NM_001318908.1:c.635_636dup	NP_001305837.1:p.Thr213GlyfsTer?
NM_007109.3:c.635_636dup MANE Select	NP_009040.2:p.Thr213GlyfsTer?
NM_001077511.2:c.635_636dup	NP_001070979.1:p.Thr213GlyfsTer?
NM_001318908.2:c.635_636dup	NP_001305837.1:p.Thr213GlyfsTer?