Canonical Allele Identifier: CA363317582
Gene: TCF19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31161732T>C , CM000668.2:g.31161732T>C GRCh38
NC_000006.11:g.31129509T>C , CM000668.1:g.31129509T>C GRCh37
NC_000006.10:g.31237488T>C NCBI36
NG_054878.1:g.1507A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000542218.2:c.524T>C ENSP00000439397.2:p.Ile175Thr
ENST00000706778.1:c.524T>C ENSP00000516543.1:p.Ile175Thr
ENST00000706779.1:c.524T>C ENSP00000516544.1:p.Ile175Thr
ENST00000706780.1:c.524T>C ENSP00000516545.1:p.Ile175Thr
ENST00000706781.1:c.524T>C ENSP00000516546.1:p.Ile175Thr
ENST00000706782.1:c.524T>C ENSP00000516547.1:p.Ile175Thr
ENST00000706783.1:c.370-15T>C ENSP00000516548.1:n.370-15T>C
ENST00000706785.1:c.370-61T>C ENSP00000516549.1:n.370-61T>C
ENST00000706786.1:c.370-15T>C ENSP00000516550.1:n.370-15T>C
ENST00000706787.1:c.524T>C ENSP00000516551.1:p.Ile175Thr
ENST00000706788.1:n.475T>C
ENST00000376257.8:c.524T>C MANE Select ENSP00000365433.3:p.Ile175Thr
ENST00000376255.4:c.524T>C ENSP00000365431.4:p.Ile175Thr
ENST00000376257.7:c.524T>C ENSP00000365433.3:p.Ile175Thr
ENST00000496421.1:n.95-19T>C
ENST00000542218.1:c.284T>C ENSP00000439397.1:p.Ile95Thr
NM_001077511.1:c.524T>C NP_001070979.1:p.Ile175Thr
NM_007109.2:c.524T>C NP_009040.2:p.Ile175Thr
XM_005249334.2:c.524T>C XP_005249391.1:p.Ile175Thr
XM_011514829.1:c.524T>C XP_011513131.1:p.Ile175Thr
NM_001318908.1:c.524T>C NP_001305837.1:p.Ile175Thr
NM_007109.3:c.524T>C MANE Select NP_009040.2:p.Ile175Thr
NM_001077511.2:c.524T>C NP_001070979.1:p.Ile175Thr
NM_001318908.2:c.524T>C NP_001305837.1:p.Ile175Thr