Canonical Allele Identifier: CA374233622

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99149214G>A , CM000671.2:g.99149214G>A	GRCh38
NC_000009.11:g.101911496G>A , CM000671.1:g.101911496G>A	GRCh37
NC_000009.10:g.100951317G>A	NCBI36
NG_007461.1:g.49085G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.1214G>A	ENSP00000449934.2:p.Cys405Tyr
ENST00000552573.7:c.1226G>A	ENSP00000447182.3:p.Cys409Tyr
ENST00000548365.6:c.*343G>A	ENSP00000448518.2:n.*343G>A
ENST00000549021.6:c.983G>A	ENSP00000449028.2:p.Cys328Tyr
ENST00000698941.1:c.1226G>A	ENSP00000514048.1:p.Cys409Tyr
ENST00000698942.1:c.*1217G>A	ENSP00000514049.1:n.*1217G>A
ENST00000698943.1:n.988G>A
ENST00000374994.9:c.1421G>A MANE Select	ENSP00000364133.4:p.Cys474Tyr
ENST00000374990.6:c.1190G>A	ENSP00000364129.2:p.Cys397Tyr
ENST00000374994.8:c.1421G>A	ENSP00000364133.4:p.Cys474Tyr
ENST00000549766.5:c.*156G>A	ENSP00000446685.1:n.*156G>A
ENST00000550253.1:c.1214G>A	ENSP00000450052.1:p.Cys405Tyr
ENST00000552516.5:c.1433G>A	ENSP00000447297.1:p.Cys478Tyr
NM_001130916.1:c.1190G>A	NP_001124388.1:p.Cys397Tyr
NM_001130916.2:c.1190G>A	NP_001124388.1:p.Cys397Tyr
NM_001306210.1:c.1433G>A	NP_001293139.1:p.Cys478Tyr
NM_004612.2:c.1421G>A	NP_004603.1:p.Cys474Tyr
NM_004612.3:c.1421G>A	NP_004603.1:p.Cys474Tyr
XM_011518948.1:c.1226G>A	XP_011517250.1:p.Cys409Tyr
XM_011518949.1:c.1214G>A	XP_011517251.1:p.Cys405Tyr
XM_011518950.1:c.983G>A	XP_011517252.1:p.Cys328Tyr
XM_011518948.2:c.1226G>A	XP_011517250.1:p.Cys409Tyr
XM_011518949.2:c.1214G>A	XP_011517251.1:p.Cys405Tyr
XM_011518950.2:c.983G>A	XP_011517252.1:p.Cys328Tyr
XM_017015063.1:c.1226G>A	XP_016870552.1:p.Cys409Tyr
XM_024447658.1:c.1214G>A	XP_024303426.1:p.Cys405Tyr
NM_004612.4:c.1421G>A MANE Select	NP_004603.1:p.Cys474Tyr
NM_001130916.3:c.1190G>A	NP_001124388.1:p.Cys397Tyr
NM_001306210.2:c.1433G>A	NP_001293139.1:p.Cys478Tyr