Canonical Allele Identifier: CA466435392
Gene: TGFBR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2967447
ClinVar RCV Id: RCV003824125
dbSNP Id: rs1407502301
gnomAD v3: 9-99146584-A-G
gnomAD v4: 9-99146584-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99146584A>G , CM000671.2:g.99146584A>G GRCh38
NC_000009.11:g.101908866A>G , CM000671.1:g.101908866A>G GRCh37
NC_000009.10:g.100948687A>G NCBI36
NG_007461.1:g.46455A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000547314.6:c.1023A>G ENSP00000449934.2:p.Glu341=
ENST00000552573.7:c.1035A>G ENSP00000447182.3:p.Glu345=
ENST00000548365.6:c.*152A>G ENSP00000448518.2:n.*152A>G
ENST00000549021.6:c.792A>G ENSP00000449028.2:p.Glu264=
ENST00000698941.1:c.1035A>G ENSP00000514048.1:p.Glu345=
ENST00000698942.1:c.*1026A>G ENSP00000514049.1:n.*1026A>G
ENST00000374994.9:c.1230A>G MANE Select ENSP00000364133.4:p.Glu410=
ENST00000374990.6:c.999A>G ENSP00000364129.2:p.Glu333=
ENST00000374994.8:c.1230A>G ENSP00000364133.4:p.Glu410=
ENST00000549766.5:c.1143-1070A>G ENSP00000446685.1:n.1143-1070A>G
ENST00000550253.1:c.1023A>G ENSP00000450052.1:p.Glu341=
ENST00000552516.5:c.1242A>G ENSP00000447297.1:p.Glu414=
NM_001130916.1:c.999A>G NP_001124388.1:p.Glu333=
NM_001130916.2:c.999A>G NP_001124388.1:p.Glu333=
NM_001306210.1:c.1242A>G NP_001293139.1:p.Glu414=
NM_004612.2:c.1230A>G NP_004603.1:p.Glu410=
NM_004612.3:c.1230A>G NP_004603.1:p.Glu410=
XM_011518948.1:c.1035A>G XP_011517250.1:p.Glu345=
XM_011518949.1:c.1023A>G XP_011517251.1:p.Glu341=
XM_011518950.1:c.792A>G XP_011517252.1:p.Glu264=
XM_011518948.2:c.1035A>G XP_011517250.1:p.Glu345=
XM_011518949.2:c.1023A>G XP_011517251.1:p.Glu341=
XM_011518950.2:c.792A>G XP_011517252.1:p.Glu264=
XM_017015063.1:c.1035A>G XP_016870552.1:p.Glu345=
XM_024447658.1:c.1023A>G XP_024303426.1:p.Glu341=
NM_004612.4:c.1230A>G MANE Select NP_004603.1:p.Glu410=
NM_001130916.3:c.999A>G NP_001124388.1:p.Glu333=
NM_001306210.2:c.1242A>G NP_001293139.1:p.Glu414=