Canonical Allele Identifier: CA2578564142

Gene: TCF19

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161854_31161859del , CM000668.2:g.31161854_31161859del	GRCh38
NC_000006.11:g.31129631_31129636del , CM000668.1:g.31129631_31129636del	GRCh37
NC_000006.10:g.31237610_31237615del	NCBI36
NG_054878.1:g.1382_1387del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.646_651del	ENSP00000439397.2:p.Ser216_Ala217del
ENST00000706778.1:c.646_651del	ENSP00000516543.1:p.Ser216_Ala217del
ENST00000706779.1:c.646_651del	ENSP00000516544.1:p.Ser216_Ala217del
ENST00000706780.1:c.646_651del	ENSP00000516545.1:p.Ser216_Ala217del
ENST00000706781.1:c.646_651del	ENSP00000516546.1:p.Ser216_Ala217del
ENST00000706782.1:c.646_651del	ENSP00000516547.1:p.Ser216_Ala217del
ENST00000706783.1:c.477_482del	ENSP00000516548.1:p.Leu160_Leu161del
ENST00000706785.1:c.431_436del	ENSP00000516549.1:p.Phe144_Cys145del
ENST00000706786.1:c.477_482del	ENSP00000516550.1:p.Leu160_Leu161del
ENST00000706787.1:c.646_651del	ENSP00000516551.1:p.Ser216_Ala217del
ENST00000706788.1:n.597_602del
ENST00000376257.8:c.646_651del MANE Select	ENSP00000365433.3:p.Ser216_Ala217del
ENST00000376255.4:c.646_651del	ENSP00000365431.4:p.Ser216_Ala217del
ENST00000376257.7:c.646_651del	ENSP00000365433.3:p.Ser216_Ala217del
ENST00000496421.1:n.198_203del
ENST00000542218.1:c.406_411del	ENSP00000439397.1:p.Ser136_Ala137del
NM_001077511.1:c.646_651del	NP_001070979.1:p.Ser216_Ala217del
NM_007109.2:c.646_651del	NP_009040.2:p.Ser216_Ala217del
XM_005249334.2:c.646_651del	XP_005249391.1:p.Ser216_Ala217del
XM_011514829.1:c.646_651del	XP_011513131.1:p.Ser216_Ala217del
NM_001318908.1:c.646_651del	NP_001305837.1:p.Ser216_Ala217del
NM_007109.3:c.646_651del MANE Select	NP_009040.2:p.Ser216_Ala217del
NM_001077511.2:c.646_651del	NP_001070979.1:p.Ser216_Ala217del
NM_001318908.2:c.646_651del	NP_001305837.1:p.Ser216_Ala217del