Canonical Allele Identifier: CA363318150
Gene: TCF19 HGNC NCBI

Linked Data

gnomAD v4: 6-31161846-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31161846C>A , CM000668.2:g.31161846C>A GRCh38
NC_000006.11:g.31129623C>A , CM000668.1:g.31129623C>A GRCh37
NC_000006.10:g.31237602C>A NCBI36
NG_054878.1:g.1393G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000542218.2:c.638C>A ENSP00000439397.2:p.Thr213Asn
ENST00000706778.1:c.638C>A ENSP00000516543.1:p.Thr213Asn
ENST00000706779.1:c.638C>A ENSP00000516544.1:p.Thr213Asn
ENST00000706780.1:c.638C>A ENSP00000516545.1:p.Thr213Asn
ENST00000706781.1:c.638C>A ENSP00000516546.1:p.Thr213Asn
ENST00000706782.1:c.638C>A ENSP00000516547.1:p.Thr213Asn
ENST00000706783.1:c.469C>A ENSP00000516548.1:p.Pro157Thr
ENST00000706785.1:c.423C>A ENSP00000516549.1:p.Asp141Glu
ENST00000706786.1:c.469C>A ENSP00000516550.1:p.Pro157Thr
ENST00000706787.1:c.638C>A ENSP00000516551.1:p.Thr213Asn
ENST00000706788.1:n.589C>A
ENST00000376257.8:c.638C>A MANE Select ENSP00000365433.3:p.Thr213Asn
ENST00000376255.4:c.638C>A ENSP00000365431.4:p.Thr213Asn
ENST00000376257.7:c.638C>A ENSP00000365433.3:p.Thr213Asn
ENST00000496421.1:n.190C>A
ENST00000542218.1:c.398C>A ENSP00000439397.1:p.Thr133Asn
NM_001077511.1:c.638C>A NP_001070979.1:p.Thr213Asn
NM_007109.2:c.638C>A NP_009040.2:p.Thr213Asn
XM_005249334.2:c.638C>A XP_005249391.1:p.Thr213Asn
XM_011514829.1:c.638C>A XP_011513131.1:p.Thr213Asn
NM_001318908.1:c.638C>A NP_001305837.1:p.Thr213Asn
NM_007109.3:c.638C>A MANE Select NP_009040.2:p.Thr213Asn
NM_001077511.2:c.638C>A NP_001070979.1:p.Thr213Asn
NM_001318908.2:c.638C>A NP_001305837.1:p.Thr213Asn