Canonical Allele Identifier: CA1867267053

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99149253G= , CM000671.2:g.99149253G=	GRCh38
NC_000009.11:g.101911535G= , CM000671.1:g.101911535G=	GRCh37
NC_000009.10:g.100951356G=	NCBI36
NG_007461.1:g.49124G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.1253G=	ENSP00000449934.2:p.Arg418=
ENST00000552573.7:c.1265G=	ENSP00000447182.3:p.Arg422=
ENST00000548365.6:c.*382G=	ENSP00000448518.2:n.*382G=
ENST00000549021.6:c.1022G=	ENSP00000449028.2:p.Arg341=
ENST00000698941.1:c.1265G=	ENSP00000514048.1:p.Arg422=
ENST00000698942.1:c.*1256G=	ENSP00000514049.1:n.*1256G=
ENST00000698943.1:n.1027G=
ENST00000374994.9:c.1460G= MANE Select	ENSP00000364133.4:p.Arg487=
ENST00000374990.6:c.1229G=	ENSP00000364129.2:p.Arg410=
ENST00000374994.8:c.1460G=	ENSP00000364133.4:p.Arg487=
ENST00000549766.5:c.*195G=	ENSP00000446685.1:n.*195G=
ENST00000550253.1:c.1253G=	ENSP00000450052.1:p.Arg418=
ENST00000552516.5:c.1472G=	ENSP00000447297.1:p.Arg491=
NM_001130916.1:c.1229G=	NP_001124388.1:p.Arg410=
NM_001130916.2:c.1229G=	NP_001124388.1:p.Arg410=
NM_001306210.1:c.1472G=	NP_001293139.1:p.Arg491=
NM_004612.2:c.1460G=	NP_004603.1:p.Arg487=
NM_004612.3:c.1460G=	NP_004603.1:p.Arg487=
XM_011518948.1:c.1265G=	XP_011517250.1:p.Arg422=
XM_011518949.1:c.1253G=	XP_011517251.1:p.Arg418=
XM_011518950.1:c.1022G=	XP_011517252.1:p.Arg341=
XM_011518948.2:c.1265G=	XP_011517250.1:p.Arg422=
XM_011518949.2:c.1253G=	XP_011517251.1:p.Arg418=
XM_011518950.2:c.1022G=	XP_011517252.1:p.Arg341=
XM_017015063.1:c.1265G=	XP_016870552.1:p.Arg422=
XM_024447658.1:c.1253G=	XP_024303426.1:p.Arg418=
NM_004612.4:c.1460G= MANE Select	NP_004603.1:p.Arg487=
NM_001130916.3:c.1229G=	NP_001124388.1:p.Arg410=
NM_001306210.2:c.1472G=	NP_001293139.1:p.Arg491=