Canonical Allele Identifier: CA363318091

Gene: TCF19

Linked Data

• MyVariant Identifiers: chr6:g.31129607C>G (hg19) ; chr6:g.31161830C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31161830C>G , CM000668.2:g.31161830C>G	GRCh38
NC_000006.11:g.31129607C>G , CM000668.1:g.31129607C>G	GRCh37
NC_000006.10:g.31237586C>G	NCBI36
NG_054878.1:g.1409G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542218.2:c.622C>G	ENSP00000439397.2:p.Pro208Ala
ENST00000706778.1:c.622C>G	ENSP00000516543.1:p.Pro208Ala
ENST00000706779.1:c.622C>G	ENSP00000516544.1:p.Pro208Ala
ENST00000706780.1:c.622C>G	ENSP00000516545.1:p.Pro208Ala
ENST00000706781.1:c.622C>G	ENSP00000516546.1:p.Pro208Ala
ENST00000706782.1:c.622C>G	ENSP00000516547.1:p.Pro208Ala
ENST00000706783.1:c.453C>G	ENSP00000516548.1:p.His151Gln
ENST00000706785.1:c.407C>G	ENSP00000516549.1:p.Thr136Ser
ENST00000706786.1:c.453C>G	ENSP00000516550.1:p.His151Gln
ENST00000706787.1:c.622C>G	ENSP00000516551.1:p.Pro208Ala
ENST00000706788.1:n.573C>G
ENST00000376257.8:c.622C>G MANE Select	ENSP00000365433.3:p.Pro208Ala
ENST00000376255.4:c.622C>G	ENSP00000365431.4:p.Pro208Ala
ENST00000376257.7:c.622C>G	ENSP00000365433.3:p.Pro208Ala
ENST00000496421.1:n.174C>G
ENST00000542218.1:c.382C>G	ENSP00000439397.1:p.Pro128Ala
NM_001077511.1:c.622C>G	NP_001070979.1:p.Pro208Ala
NM_007109.2:c.622C>G	NP_009040.2:p.Pro208Ala
XM_005249334.2:c.622C>G	XP_005249391.1:p.Pro208Ala
XM_011514829.1:c.622C>G	XP_011513131.1:p.Pro208Ala
NM_001318908.1:c.622C>G	NP_001305837.1:p.Pro208Ala
NM_007109.3:c.622C>G MANE Select	NP_009040.2:p.Pro208Ala
NM_001077511.2:c.622C>G	NP_001070979.1:p.Pro208Ala
NM_001318908.2:c.622C>G	NP_001305837.1:p.Pro208Ala