Canonical Allele Identifier: CA1867260109

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142619G= , CM000671.2:g.99142619G=	GRCh38
NC_000009.11:g.101904901G= , CM000671.1:g.101904901G=	GRCh37
NC_000009.10:g.100944722G=	NCBI36
NG_007461.1:g.42490G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.682G=	ENSP00000449934.2:p.Val228=
ENST00000552573.7:c.694G=	ENSP00000447182.3:p.Val232=
ENST00000548365.6:c.463G=	ENSP00000448518.2:p.Val155=
ENST00000549021.6:c.451G=	ENSP00000449028.2:p.Val151=
ENST00000698941.1:c.694G=	ENSP00000514048.1:p.Val232=
ENST00000698942.1:c.*685G=	ENSP00000514049.1:n.*685G=
ENST00000374994.9:c.889G= MANE Select	ENSP00000364133.4:p.Val297=
ENST00000374990.6:c.658G=	ENSP00000364129.2:p.Val220=
ENST00000374994.8:c.889G=	ENSP00000364133.4:p.Val297=
ENST00000549766.5:c.901G=	ENSP00000446685.1:p.Val301=
ENST00000550253.1:c.682G=	ENSP00000450052.1:p.Val228=
ENST00000552516.5:c.901G=	ENSP00000447297.1:p.Val301=
NM_001130916.1:c.658G=	NP_001124388.1:p.Val220=
NM_001130916.2:c.658G=	NP_001124388.1:p.Val220=
NM_001306210.1:c.901G=	NP_001293139.1:p.Val301=
NM_004612.2:c.889G=	NP_004603.1:p.Val297=
NM_004612.3:c.889G=	NP_004603.1:p.Val297=
XM_011518948.1:c.694G=	XP_011517250.1:p.Val232=
XM_011518949.1:c.682G=	XP_011517251.1:p.Val228=
XM_011518950.1:c.451G=	XP_011517252.1:p.Val151=
XM_011518948.2:c.694G=	XP_011517250.1:p.Val232=
XM_011518949.2:c.682G=	XP_011517251.1:p.Val228=
XM_011518950.2:c.451G=	XP_011517252.1:p.Val151=
XM_017015063.1:c.694G=	XP_016870552.1:p.Val232=
XM_024447658.1:c.682G=	XP_024303426.1:p.Val228=
NM_004612.4:c.889G= MANE Select	NP_004603.1:p.Val297=
NM_001130916.3:c.658G=	NP_001124388.1:p.Val220=
NM_001306210.2:c.901G=	NP_001293139.1:p.Val301=