Canonical Allele Identifier: CA1867263956
Gene: TGFBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99146591C= , CM000671.2:g.99146591C= GRCh38
NC_000009.11:g.101908873C= , CM000671.1:g.101908873C= GRCh37
NC_000009.10:g.100948694C= NCBI36
NG_007461.1:g.46462C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547314.6:c.1030C= ENSP00000449934.2:p.Arg344=
ENST00000552573.7:c.1042C= ENSP00000447182.3:p.Arg348=
ENST00000548365.6:c.*159C= ENSP00000448518.2:n.*159C=
ENST00000549021.6:c.799C= ENSP00000449028.2:p.Arg267=
ENST00000698941.1:c.1042C= ENSP00000514048.1:p.Arg348=
ENST00000698942.1:c.*1033C= ENSP00000514049.1:n.*1033C=
ENST00000374994.9:c.1237C= MANE Select ENSP00000364133.4:p.Arg413=
ENST00000374990.6:c.1006C= ENSP00000364129.2:p.Arg336=
ENST00000374994.8:c.1237C= ENSP00000364133.4:p.Arg413=
ENST00000549766.5:c.1143-1063C= ENSP00000446685.1:n.1143-1063C=
ENST00000550253.1:c.1030C= ENSP00000450052.1:p.Arg344=
ENST00000552516.5:c.1249C= ENSP00000447297.1:p.Arg417=
NM_001130916.1:c.1006C= NP_001124388.1:p.Arg336=
NM_001130916.2:c.1006C= NP_001124388.1:p.Arg336=
NM_001306210.1:c.1249C= NP_001293139.1:p.Arg417=
NM_004612.2:c.1237C= NP_004603.1:p.Arg413=
NM_004612.3:c.1237C= NP_004603.1:p.Arg413=
XM_011518948.1:c.1042C= XP_011517250.1:p.Arg348=
XM_011518949.1:c.1030C= XP_011517251.1:p.Arg344=
XM_011518950.1:c.799C= XP_011517252.1:p.Arg267=
XM_011518948.2:c.1042C= XP_011517250.1:p.Arg348=
XM_011518949.2:c.1030C= XP_011517251.1:p.Arg344=
XM_011518950.2:c.799C= XP_011517252.1:p.Arg267=
XM_017015063.1:c.1042C= XP_016870552.1:p.Arg348=
XM_024447658.1:c.1030C= XP_024303426.1:p.Arg344=
NM_004612.4:c.1237C= MANE Select NP_004603.1:p.Arg413=
NM_001130916.3:c.1006C= NP_001124388.1:p.Arg336=
NM_001306210.2:c.1249C= NP_001293139.1:p.Arg417=