Canonical Allele Identifier: CA363318454

Gene: TCF19

Linked Data

• MyVariant Identifiers: chr6:g.31129766C>T (hg19) ; chr6:g.31161989C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161989C>T , CM000668.2:g.31161989C>T	GRCh38
NC_000006.11:g.31129766C>T , CM000668.1:g.31129766C>T	GRCh37
NC_000006.10:g.31237745C>T	NCBI36
NG_054878.1:g.1250G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.781C>T	ENSP00000439397.2:p.Pro261Ser
ENST00000706778.1:c.781C>T	ENSP00000516543.1:p.Pro261Ser
ENST00000706779.1:c.781C>T	ENSP00000516544.1:p.Pro261Ser
ENST00000706780.1:c.781C>T	ENSP00000516545.1:p.Pro261Ser
ENST00000706781.1:c.781C>T	ENSP00000516546.1:p.Pro261Ser
ENST00000706782.1:c.781C>T	ENSP00000516547.1:p.Pro261Ser
ENST00000706783.1:c.*9C>T	ENSP00000516548.1:n.*9C>T
ENST00000706785.1:c.*74C>T	ENSP00000516549.1:n.*74C>T
ENST00000706786.1:c.*9C>T	ENSP00000516550.1:n.*9C>T
ENST00000706787.1:c.781C>T	ENSP00000516551.1:p.Pro261Ser
ENST00000706788.1:n.732C>T
ENST00000376257.8:c.781C>T MANE Select	ENSP00000365433.3:p.Pro261Ser
ENST00000376255.4:c.781C>T	ENSP00000365431.4:p.Pro261Ser
ENST00000376257.7:c.781C>T	ENSP00000365433.3:p.Pro261Ser
ENST00000496421.1:n.333C>T
ENST00000542218.1:c.541C>T	ENSP00000439397.1:p.Pro181Ser
NM_001077511.1:c.781C>T	NP_001070979.1:p.Pro261Ser
NM_007109.2:c.781C>T	NP_009040.2:p.Pro261Ser
XM_005249334.2:c.781C>T	XP_005249391.1:p.Pro261Ser
XM_011514829.1:c.781C>T	XP_011513131.1:p.Pro261Ser
NM_001318908.1:c.781C>T	NP_001305837.1:p.Pro261Ser
NM_007109.3:c.781C>T MANE Select	NP_009040.2:p.Pro261Ser
NM_001077511.2:c.781C>T	NP_001070979.1:p.Pro261Ser
NM_001318908.2:c.781C>T	NP_001305837.1:p.Pro261Ser