Canonical Allele Identifier: CA1867260157

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142656C= , CM000671.2:g.99142656C=	GRCh38
NC_000009.11:g.101904938C= , CM000671.1:g.101904938C=	GRCh37
NC_000009.10:g.100944759C=	NCBI36
NG_007461.1:g.42527C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.719C=	ENSP00000449934.2:p.Thr240=
ENST00000552573.7:c.731C=	ENSP00000447182.3:p.Thr244=
ENST00000548365.6:c.500C=	ENSP00000448518.2:p.Thr167=
ENST00000549021.6:c.488C=	ENSP00000449028.2:p.Thr163=
ENST00000698941.1:c.731C=	ENSP00000514048.1:p.Thr244=
ENST00000698942.1:c.*722C=	ENSP00000514049.1:n.*722C=
ENST00000374994.9:c.926C= MANE Select	ENSP00000364133.4:p.Thr309=
ENST00000374990.6:c.695C=	ENSP00000364129.2:p.Thr232=
ENST00000374994.8:c.926C=	ENSP00000364133.4:p.Thr309=
ENST00000549766.5:c.938C=	ENSP00000446685.1:p.Thr313=
ENST00000550253.1:c.719C=	ENSP00000450052.1:p.Thr240=
ENST00000552516.5:c.938C=	ENSP00000447297.1:p.Thr313=
NM_001130916.1:c.695C=	NP_001124388.1:p.Thr232=
NM_001130916.2:c.695C=	NP_001124388.1:p.Thr232=
NM_001306210.1:c.938C=	NP_001293139.1:p.Thr313=
NM_004612.2:c.926C=	NP_004603.1:p.Thr309=
NM_004612.3:c.926C=	NP_004603.1:p.Thr309=
XM_011518948.1:c.731C=	XP_011517250.1:p.Thr244=
XM_011518949.1:c.719C=	XP_011517251.1:p.Thr240=
XM_011518950.1:c.488C=	XP_011517252.1:p.Thr163=
XM_011518948.2:c.731C=	XP_011517250.1:p.Thr244=
XM_011518949.2:c.719C=	XP_011517251.1:p.Thr240=
XM_011518950.2:c.488C=	XP_011517252.1:p.Thr163=
XM_017015063.1:c.731C=	XP_016870552.1:p.Thr244=
XM_024447658.1:c.719C=	XP_024303426.1:p.Thr240=
NM_004612.4:c.926C= MANE Select	NP_004603.1:p.Thr309=
NM_001130916.3:c.695C=	NP_001124388.1:p.Thr232=
NM_001306210.2:c.938C=	NP_001293139.1:p.Thr313=