Canonical Allele Identifier: CA374230821
Gene: TGFBR1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1393030
ClinVar RCV Id: RCV001912468
dbSNP Id: rs1827655038
gnomAD v3: 9-99142691-G-T
gnomAD v4: 9-99142691-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99142691G>T , CM000671.2:g.99142691G>T GRCh38
NC_000009.11:g.101904973G>T , CM000671.1:g.101904973G>T GRCh37
NC_000009.10:g.100944794G>T NCBI36
NG_007461.1:g.42562G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000547314.6:c.754G>T ENSP00000449934.2:p.Val252Phe
ENST00000552573.7:c.766G>T ENSP00000447182.3:p.Val256Phe
ENST00000548365.6:c.535G>T ENSP00000448518.2:p.Val179Phe
ENST00000549021.6:c.523G>T ENSP00000449028.2:p.Val175Phe
ENST00000698941.1:c.766G>T ENSP00000514048.1:p.Val256Phe
ENST00000698942.1:c.*757G>T ENSP00000514049.1:n.*757G>T
ENST00000374994.9:c.961G>T MANE Select ENSP00000364133.4:p.Val321Phe
ENST00000374990.6:c.730G>T ENSP00000364129.2:p.Val244Phe
ENST00000374994.8:c.961G>T ENSP00000364133.4:p.Val321Phe
ENST00000549766.5:c.973G>T ENSP00000446685.1:p.Val325Phe
ENST00000550253.1:c.754G>T ENSP00000450052.1:p.Val252Phe
ENST00000552516.5:c.973G>T ENSP00000447297.1:p.Val325Phe
NM_001130916.1:c.730G>T NP_001124388.1:p.Val244Phe
NM_001130916.2:c.730G>T NP_001124388.1:p.Val244Phe
NM_001306210.1:c.973G>T NP_001293139.1:p.Val325Phe
NM_004612.2:c.961G>T NP_004603.1:p.Val321Phe
NM_004612.3:c.961G>T NP_004603.1:p.Val321Phe
XM_011518948.1:c.766G>T XP_011517250.1:p.Val256Phe
XM_011518949.1:c.754G>T XP_011517251.1:p.Val252Phe
XM_011518950.1:c.523G>T XP_011517252.1:p.Val175Phe
XM_011518948.2:c.766G>T XP_011517250.1:p.Val256Phe
XM_011518949.2:c.754G>T XP_011517251.1:p.Val252Phe
XM_011518950.2:c.523G>T XP_011517252.1:p.Val175Phe
XM_017015063.1:c.766G>T XP_016870552.1:p.Val256Phe
XM_024447658.1:c.754G>T XP_024303426.1:p.Val252Phe
NM_004612.4:c.961G>T MANE Select NP_004603.1:p.Val321Phe
NM_001130916.3:c.730G>T NP_001124388.1:p.Val244Phe
NM_001306210.2:c.973G>T NP_001293139.1:p.Val325Phe