Canonical Allele Identifier: CA466434157

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101900184G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99137902G>A , CM000671.2:g.99137902G>A	GRCh38
NC_000009.11:g.101900184G>A , CM000671.1:g.101900184G>A	GRCh37
NC_000009.10:g.100940005G>A	NCBI36
NG_007461.1:g.37773G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.411G>A	ENSP00000449934.2:p.Val137=
ENST00000552573.7:c.423G>A	ENSP00000447182.3:p.Val141=
ENST00000548365.6:c.380-4634G>A	ENSP00000448518.2:n.380-4634G>A
ENST00000549021.6:c.180G>A	ENSP00000449028.2:p.Val60=
ENST00000698941.1:c.423G>A	ENSP00000514048.1:p.Val141=
ENST00000698942.1:c.*414G>A	ENSP00000514049.1:n.*414G>A
ENST00000374994.9:c.618G>A MANE Select	ENSP00000364133.4:p.Val206=
ENST00000374990.6:c.387G>A	ENSP00000364129.2:p.Val129=
ENST00000374994.8:c.618G>A	ENSP00000364133.4:p.Val206=
ENST00000549021.5:c.180G>A	ENSP00000449028.1:p.Val60=
ENST00000549766.5:c.630G>A	ENSP00000446685.1:p.Val210=
ENST00000550253.1:c.411G>A	ENSP00000450052.1:p.Val137=
ENST00000552516.5:c.630G>A	ENSP00000447297.1:p.Val210=
NM_001130916.1:c.387G>A	NP_001124388.1:p.Val129=
NM_001130916.2:c.387G>A	NP_001124388.1:p.Val129=
NM_001306210.1:c.630G>A	NP_001293139.1:p.Val210=
NM_004612.2:c.618G>A	NP_004603.1:p.Val206=
NM_004612.3:c.618G>A	NP_004603.1:p.Val206=
XM_011518948.1:c.423G>A	XP_011517250.1:p.Val141=
XM_011518949.1:c.411G>A	XP_011517251.1:p.Val137=
XM_011518950.1:c.180G>A	XP_011517252.1:p.Val60=
XM_011518948.2:c.423G>A	XP_011517250.1:p.Val141=
XM_011518949.2:c.411G>A	XP_011517251.1:p.Val137=
XM_011518950.2:c.180G>A	XP_011517252.1:p.Val60=
XM_017015063.1:c.423G>A	XP_016870552.1:p.Val141=
XM_024447658.1:c.411G>A	XP_024303426.1:p.Val137=
NM_004612.4:c.618G>A MANE Select	NP_004603.1:p.Val206=
NM_001130916.3:c.387G>A	NP_001124388.1:p.Val129=
NM_001306210.2:c.630G>A	NP_001293139.1:p.Val210=