Canonical Allele Identifier: CA363318486

Gene: TCF19

Linked Data

• MyVariant Identifiers: chr6:g.31129783G>C (hg19) ; chr6:g.31162006G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31162006G>C , CM000668.2:g.31162006G>C	GRCh38
NC_000006.11:g.31129783G>C , CM000668.1:g.31129783G>C	GRCh37
NC_000006.10:g.31237762G>C	NCBI36
NG_054878.1:g.1233C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542218.2:c.797+1G>C	ENSP00000439397.2:n.797+1G>C
ENST00000706778.1:c.797+1G>C	ENSP00000516543.1:n.797+1G>C
ENST00000706779.1:c.797+1G>C	ENSP00000516544.1:n.797+1G>C
ENST00000706780.1:c.797+1G>C	ENSP00000516545.1:n.797+1G>C
ENST00000706781.1:c.797+1G>C	ENSP00000516546.1:n.797+1G>C
ENST00000706782.1:c.797+1G>C	ENSP00000516547.1:n.797+1G>C
ENST00000706783.1:c.*25+1G>C	ENSP00000516548.1:n.*25+1G>C
ENST00000706785.1:c.*90+1G>C	ENSP00000516549.1:n.*90+1G>C
ENST00000706786.1:c.*25+1G>C	ENSP00000516550.1:n.*25+1G>C
ENST00000706787.1:c.797+1G>C	ENSP00000516551.1:n.797+1G>C
ENST00000706788.1:n.748+1G>C
ENST00000376257.8:c.797+1G>C MANE Select	ENSP00000365433.3:n.797+1G>C
ENST00000376255.4:c.797+1G>C	ENSP00000365431.4:n.797+1G>C
ENST00000376257.7:c.797+1G>C	ENSP00000365433.3:n.797+1G>C
ENST00000496421.1:n.349+1G>C
ENST00000542218.1:c.557+1G>C	ENSP00000439397.1:n.557+1G>C
NM_001077511.1:c.797+1G>C	NP_001070979.1:n.797+1G>C
NM_007109.2:c.797+1G>C	NP_009040.2:n.797+1G>C
XM_005249334.2:c.797+1G>C	XP_005249391.1:n.797+1G>C
XM_011514829.1:c.797+1G>C	XP_011513131.1:n.797+1G>C
NM_001318908.1:c.797+1G>C	NP_001305837.1:n.797+1G>C
NM_007109.3:c.797+1G>C MANE Select	NP_009040.2:n.797+1G>C
NM_001077511.2:c.797+1G>C	NP_001070979.1:n.797+1G>C
NM_001318908.2:c.797+1G>C	NP_001305837.1:n.797+1G>C