Canonical Allele Identifier: CA363318461

Gene: TCF19

Linked Data

• MyVariant Identifiers: chr6:g.31129770T>G (hg19) ; chr6:g.31161993T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161993T>G , CM000668.2:g.31161993T>G	GRCh38
NC_000006.11:g.31129770T>G , CM000668.1:g.31129770T>G	GRCh37
NC_000006.10:g.31237749T>G	NCBI36
NG_054878.1:g.1246A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.785T>G	ENSP00000439397.2:p.Leu262Arg
ENST00000706778.1:c.785T>G	ENSP00000516543.1:p.Leu262Arg
ENST00000706779.1:c.785T>G	ENSP00000516544.1:p.Leu262Arg
ENST00000706780.1:c.785T>G	ENSP00000516545.1:p.Leu262Arg
ENST00000706781.1:c.785T>G	ENSP00000516546.1:p.Leu262Arg
ENST00000706782.1:c.785T>G	ENSP00000516547.1:p.Leu262Arg
ENST00000706783.1:c.*13T>G	ENSP00000516548.1:n.*13T>G
ENST00000706785.1:c.*78T>G	ENSP00000516549.1:n.*78T>G
ENST00000706786.1:c.*13T>G	ENSP00000516550.1:n.*13T>G
ENST00000706787.1:c.785T>G	ENSP00000516551.1:p.Leu262Arg
ENST00000706788.1:n.736T>G
ENST00000376257.8:c.785T>G MANE Select	ENSP00000365433.3:p.Leu262Arg
ENST00000376255.4:c.785T>G	ENSP00000365431.4:p.Leu262Arg
ENST00000376257.7:c.785T>G	ENSP00000365433.3:p.Leu262Arg
ENST00000496421.1:n.337T>G
ENST00000542218.1:c.545T>G	ENSP00000439397.1:p.Leu182Arg
NM_001077511.1:c.785T>G	NP_001070979.1:p.Leu262Arg
NM_007109.2:c.785T>G	NP_009040.2:p.Leu262Arg
XM_005249334.2:c.785T>G	XP_005249391.1:p.Leu262Arg
XM_011514829.1:c.785T>G	XP_011513131.1:p.Leu262Arg
NM_001318908.1:c.785T>G	NP_001305837.1:p.Leu262Arg
NM_007109.3:c.785T>G MANE Select	NP_009040.2:p.Leu262Arg
NM_001077511.2:c.785T>G	NP_001070979.1:p.Leu262Arg
NM_001318908.2:c.785T>G	NP_001305837.1:p.Leu262Arg