Canonical Allele Identifier: CA1619031060
Gene: TCF19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31161965_31161978delinsAAGAAACTCCGTGT , CM000668.2:g.31161965_31161978delinsAAGAAACTCCGTGT GRCh38
NC_000006.11:g.31129742_31129755delinsAAGAAACTCCGTGT , CM000668.1:g.31129742_31129755delinsAAGAAACTCCGTGT GRCh37
NC_000006.10:g.31237721_31237734delinsAAGAAACTCCGTGT NCBI36
NG_054878.1:g.1261_1274delinsACACGGAGTTTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000542218.2:c.757_770delinsAAGAAACTCCGTGT ENSP00000439397.2:p.Lys253=
ENST00000706778.1:c.757_770delinsAAGAAACTCCGTGT ENSP00000516543.1:p.Lys253=
ENST00000706779.1:c.757_770delinsAAGAAACTCCGTGT ENSP00000516544.1:p.Lys253=
ENST00000706780.1:c.757_770delinsAAGAAACTCCGTGT ENSP00000516545.1:p.Lys253=
ENST00000706781.1:c.757_770delinsAAGAAACTCCGTGT ENSP00000516546.1:p.Lys253=
ENST00000706782.1:c.757_770delinsAAGAAACTCCGTGT ENSP00000516547.1:p.Lys253=
ENST00000706783.1:c.588_601delinsAAGAAACTCCGTGT ENSP00000516548.1:p.Gly196=
ENST00000706785.1:c.*50_*63delinsAAGAAACTCCGTGT ENSP00000516549.1:n.*50_*63delinsAAGAAACTCCGTGT
ENST00000706786.1:c.588_601delinsAAGAAACTCCGTGT ENSP00000516550.1:p.Gly196=
ENST00000706787.1:c.757_770delinsAAGAAACTCCGTGT ENSP00000516551.1:p.Lys253=
ENST00000706788.1:n.708_721delinsAAGAAACTCCGTGT
ENST00000376257.8:c.757_770delinsAAGAAACTCCGTGT MANE Select ENSP00000365433.3:p.Lys253=
ENST00000376255.4:c.757_770delinsAAGAAACTCCGTGT ENSP00000365431.4:p.Lys253=
ENST00000376257.7:c.757_770delinsAAGAAACTCCGTGT ENSP00000365433.3:p.Lys253=
ENST00000496421.1:n.309_322delinsAAGAAACTCCGTGT
ENST00000542218.1:c.517_530delinsAAGAAACTCCGTGT ENSP00000439397.1:p.Lys173=
NM_001077511.1:c.757_770delinsAAGAAACTCCGTGT NP_001070979.1:p.Lys253=
NM_007109.2:c.757_770delinsAAGAAACTCCGTGT NP_009040.2:p.Lys253=
XM_005249334.2:c.757_770delinsAAGAAACTCCGTGT XP_005249391.1:p.Lys253=
XM_011514829.1:c.757_770delinsAAGAAACTCCGTGT XP_011513131.1:p.Lys253=
NM_001318908.1:c.757_770delinsAAGAAACTCCGTGT NP_001305837.1:p.Lys253=
NM_007109.3:c.757_770delinsAAGAAACTCCGTGT MANE Select NP_009040.2:p.Lys253=
NM_001077511.2:c.757_770delinsAAGAAACTCCGTGT NP_001070979.1:p.Lys253=
NM_001318908.2:c.757_770delinsAAGAAACTCCGTGT NP_001305837.1:p.Lys253=