Canonical Allele Identifier: CA374230690
Gene: TGFBR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99142629A>C , CM000671.2:g.99142629A>C GRCh38
NC_000009.11:g.101904911A>C , CM000671.1:g.101904911A>C GRCh37
NC_000009.10:g.100944732A>C NCBI36
NG_007461.1:g.42500A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000547314.6:c.692A>C ENSP00000449934.2:p.Glu231Ala
ENST00000552573.7:c.704A>C ENSP00000447182.3:p.Glu235Ala
ENST00000548365.6:c.473A>C ENSP00000448518.2:p.Glu158Ala
ENST00000549021.6:c.461A>C ENSP00000449028.2:p.Glu154Ala
ENST00000698941.1:c.704A>C ENSP00000514048.1:p.Glu235Ala
ENST00000698942.1:c.*695A>C ENSP00000514049.1:n.*695A>C
ENST00000374994.9:c.899A>C MANE Select ENSP00000364133.4:p.Glu300Ala
ENST00000374990.6:c.668A>C ENSP00000364129.2:p.Glu223Ala
ENST00000374994.8:c.899A>C ENSP00000364133.4:p.Glu300Ala
ENST00000549766.5:c.911A>C ENSP00000446685.1:p.Glu304Ala
ENST00000550253.1:c.692A>C ENSP00000450052.1:p.Glu231Ala
ENST00000552516.5:c.911A>C ENSP00000447297.1:p.Glu304Ala
NM_001130916.1:c.668A>C NP_001124388.1:p.Glu223Ala
NM_001130916.2:c.668A>C NP_001124388.1:p.Glu223Ala
NM_001306210.1:c.911A>C NP_001293139.1:p.Glu304Ala
NM_004612.2:c.899A>C NP_004603.1:p.Glu300Ala
NM_004612.3:c.899A>C NP_004603.1:p.Glu300Ala
XM_011518948.1:c.704A>C XP_011517250.1:p.Glu235Ala
XM_011518949.1:c.692A>C XP_011517251.1:p.Glu231Ala
XM_011518950.1:c.461A>C XP_011517252.1:p.Glu154Ala
XM_011518948.2:c.704A>C XP_011517250.1:p.Glu235Ala
XM_011518949.2:c.692A>C XP_011517251.1:p.Glu231Ala
XM_011518950.2:c.461A>C XP_011517252.1:p.Glu154Ala
XM_017015063.1:c.704A>C XP_016870552.1:p.Glu235Ala
XM_024447658.1:c.692A>C XP_024303426.1:p.Glu231Ala
NM_004612.4:c.899A>C MANE Select NP_004603.1:p.Glu300Ala
NM_001130916.3:c.668A>C NP_001124388.1:p.Glu223Ala
NM_001306210.2:c.911A>C NP_001293139.1:p.Glu304Ala