Canonical Allele Identifier: CA1619030965
Gene: TCF19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31161749A= , CM000668.2:g.31161749A= GRCh38
NC_000006.11:g.31129526A= , CM000668.1:g.31129526A= GRCh37
NC_000006.10:g.31237505A= NCBI36
NG_054878.1:g.1490T=

Transcript Alleles

HGVS Amino-acid change
ENST00000542218.2:c.541A= ENSP00000439397.2:p.Ser181=
ENST00000706778.1:c.541A= ENSP00000516543.1:p.Ser181=
ENST00000706779.1:c.541A= ENSP00000516544.1:p.Ser181=
ENST00000706780.1:c.541A= ENSP00000516545.1:p.Ser181=
ENST00000706781.1:c.541A= ENSP00000516546.1:p.Ser181=
ENST00000706782.1:c.541A= ENSP00000516547.1:p.Ser181=
ENST00000706783.1:c.372A= ENSP00000516548.1:p.Ala124=
ENST00000706785.1:c.370-44A= ENSP00000516549.1:n.370-44A=
ENST00000706786.1:c.372A= ENSP00000516550.1:p.Ala124=
ENST00000706787.1:c.541A= ENSP00000516551.1:p.Ser181=
ENST00000706788.1:n.492A=
ENST00000376257.8:c.541A= MANE Select ENSP00000365433.3:p.Ser181=
ENST00000376255.4:c.541A= ENSP00000365431.4:p.Ser181=
ENST00000376257.7:c.541A= ENSP00000365433.3:p.Ser181=
ENST00000496421.1:n.95-2A=
ENST00000542218.1:c.301A= ENSP00000439397.1:p.Ser101=
NM_001077511.1:c.541A= NP_001070979.1:p.Ser181=
NM_007109.2:c.541A= NP_009040.2:p.Ser181=
XM_005249334.2:c.541A= XP_005249391.1:p.Ser181=
XM_011514829.1:c.541A= XP_011513131.1:p.Ser181=
NM_001318908.1:c.541A= NP_001305837.1:p.Ser181=
NM_007109.3:c.541A= MANE Select NP_009040.2:p.Ser181=
NM_001077511.2:c.541A= NP_001070979.1:p.Ser181=
NM_001318908.2:c.541A= NP_001305837.1:p.Ser181=