Canonical Allele Identifier: CA363318097
Gene: TCF19 HGNC NCBI

Linked Data

gnomAD v4: 6-31161831-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31161831C>T , CM000668.2:g.31161831C>T GRCh38
NC_000006.11:g.31129608C>T , CM000668.1:g.31129608C>T GRCh37
NC_000006.10:g.31237587C>T NCBI36
NG_054878.1:g.1408G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000542218.2:c.623C>T ENSP00000439397.2:p.Pro208Leu
ENST00000706778.1:c.623C>T ENSP00000516543.1:p.Pro208Leu
ENST00000706779.1:c.623C>T ENSP00000516544.1:p.Pro208Leu
ENST00000706780.1:c.623C>T ENSP00000516545.1:p.Pro208Leu
ENST00000706781.1:c.623C>T ENSP00000516546.1:p.Pro208Leu
ENST00000706782.1:c.623C>T ENSP00000516547.1:p.Pro208Leu
ENST00000706783.1:c.454C>T ENSP00000516548.1:p.Leu152=
ENST00000706785.1:c.408C>T ENSP00000516549.1:p.Thr136=
ENST00000706786.1:c.454C>T ENSP00000516550.1:p.Leu152=
ENST00000706787.1:c.623C>T ENSP00000516551.1:p.Pro208Leu
ENST00000706788.1:n.574C>T
ENST00000376257.8:c.623C>T MANE Select ENSP00000365433.3:p.Pro208Leu
ENST00000376255.4:c.623C>T ENSP00000365431.4:p.Pro208Leu
ENST00000376257.7:c.623C>T ENSP00000365433.3:p.Pro208Leu
ENST00000496421.1:n.175C>T
ENST00000542218.1:c.383C>T ENSP00000439397.1:p.Pro128Leu
NM_001077511.1:c.623C>T NP_001070979.1:p.Pro208Leu
NM_007109.2:c.623C>T NP_009040.2:p.Pro208Leu
XM_005249334.2:c.623C>T XP_005249391.1:p.Pro208Leu
XM_011514829.1:c.623C>T XP_011513131.1:p.Pro208Leu
NM_001318908.1:c.623C>T NP_001305837.1:p.Pro208Leu
NM_007109.3:c.623C>T MANE Select NP_009040.2:p.Pro208Leu
NM_001077511.2:c.623C>T NP_001070979.1:p.Pro208Leu
NM_001318908.2:c.623C>T NP_001305837.1:p.Pro208Leu