Canonical Allele Identifier: CA3709688

Gene: TCF19

Linked Data

• dbSNP Id: rs756033523
• ExAC: 6:31129514 A / AGTGGTAGAGCTAGGATCTGAACG
• MyVariant Identifiers: chr6:g.31129514_31129515insGTGGTAGAGCTAGGATCTGAACG (hg19) ; chr6:g.31161737_31161738insGTGGTAGAGCTAGGATCTGAACG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161737_31161738insGTGGTAGAGCTAGGATCTGAACG , CM000668.2:g.31161737_31161738insGTGGTAGAGCTAGGATCTGAACG	GRCh38
NC_000006.11:g.31129514_31129515insGTGGTAGAGCTAGGATCTGAACG , CM000668.1:g.31129514_31129515insGTGGTAGAGCTAGGATCTGAACG	GRCh37
NC_000006.10:g.31237493_31237494insGTGGTAGAGCTAGGATCTGAACG	NCBI36
NG_054878.1:g.1501_1502insCGTTCAGATCCTAGCTCTACCAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000542218.2:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000439397.2:p.Asn177SerfsTer7
ENST00000706778.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516543.1:p.Asn177SerfsTer7
ENST00000706779.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516544.1:p.Asn177SerfsTer7
ENST00000706780.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516545.1:p.Asn177SerfsTer7
ENST00000706781.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516546.1:p.Asn177SerfsTer7
ENST00000706782.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516547.1:p.Asn177SerfsTer7
ENST00000706783.1:c.370-10_370-9insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516548.1:n.370-10_370-9insGTGGTAGAGCTAGGATCTGAACG
ENST00000706785.1:c.370-56_370-55insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516549.1:n.370-56_370-55insGTGGTAGAGCTAGGATCTGAACG
ENST00000706786.1:c.370-10_370-9insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516550.1:n.370-10_370-9insGTGGTAGAGCTAGGATCTGAACG
ENST00000706787.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000516551.1:p.Asn177SerfsTer7
ENST00000706788.1:n.480_481insGTGGTAGAGCTAGGATCTGAACG
ENST00000376257.8:c.529_530insGTGGTAGAGCTAGGATCTGAACG MANE Select	ENSP00000365433.3:p.Asn177SerfsTer7
ENST00000376255.4:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000365431.4:p.Asn177SerfsTer7
ENST00000376257.7:c.529_530insGTGGTAGAGCTAGGATCTGAACG	ENSP00000365433.3:p.Asn177SerfsTer7
ENST00000496421.1:n.95-14_95-13insGTGGTAGAGCTAGGATCTGAACG
ENST00000542218.1:c.289_290insGTGGTAGAGCTAGGATCTGAACG	ENSP00000439397.1:p.Asn97SerfsTer7
NM_001077511.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	NP_001070979.1:p.Asn177SerfsTer7
NM_007109.2:c.529_530insGTGGTAGAGCTAGGATCTGAACG	NP_009040.2:p.Asn177SerfsTer7
XM_005249334.2:c.529_530insGTGGTAGAGCTAGGATCTGAACG	XP_005249391.1:p.Asn177SerfsTer7
XM_011514829.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	XP_011513131.1:p.Asn177SerfsTer7
NM_001318908.1:c.529_530insGTGGTAGAGCTAGGATCTGAACG	NP_001305837.1:p.Asn177SerfsTer7
NM_007109.3:c.529_530insGTGGTAGAGCTAGGATCTGAACG MANE Select	NP_009040.2:p.Asn177SerfsTer7
NM_001077511.2:c.529_530insGTGGTAGAGCTAGGATCTGAACG	NP_001070979.1:p.Asn177SerfsTer7
NM_001318908.2:c.529_530insGTGGTAGAGCTAGGATCTGAACG	NP_001305837.1:p.Asn177SerfsTer7