Canonical Allele Identifier: CA466435397

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908872T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146590T>A , CM000671.2:g.99146590T>A	GRCh38
NC_000009.11:g.101908872T>A , CM000671.1:g.101908872T>A	GRCh37
NC_000009.10:g.100948693T>A	NCBI36
NG_007461.1:g.46461T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.1029T>A	ENSP00000449934.2:p.Ala343=
ENST00000552573.7:c.1041T>A	ENSP00000447182.3:p.Ala347=
ENST00000548365.6:c.*158T>A	ENSP00000448518.2:n.*158T>A
ENST00000549021.6:c.798T>A	ENSP00000449028.2:p.Ala266=
ENST00000698941.1:c.1041T>A	ENSP00000514048.1:p.Ala347=
ENST00000698942.1:c.*1032T>A	ENSP00000514049.1:n.*1032T>A
ENST00000374994.9:c.1236T>A MANE Select	ENSP00000364133.4:p.Ala412=
ENST00000374990.6:c.1005T>A	ENSP00000364129.2:p.Ala335=
ENST00000374994.8:c.1236T>A	ENSP00000364133.4:p.Ala412=
ENST00000549766.5:c.1143-1064T>A	ENSP00000446685.1:n.1143-1064T>A
ENST00000550253.1:c.1029T>A	ENSP00000450052.1:p.Ala343=
ENST00000552516.5:c.1248T>A	ENSP00000447297.1:p.Ala416=
NM_001130916.1:c.1005T>A	NP_001124388.1:p.Ala335=
NM_001130916.2:c.1005T>A	NP_001124388.1:p.Ala335=
NM_001306210.1:c.1248T>A	NP_001293139.1:p.Ala416=
NM_004612.2:c.1236T>A	NP_004603.1:p.Ala412=
NM_004612.3:c.1236T>A	NP_004603.1:p.Ala412=
XM_011518948.1:c.1041T>A	XP_011517250.1:p.Ala347=
XM_011518949.1:c.1029T>A	XP_011517251.1:p.Ala343=
XM_011518950.1:c.798T>A	XP_011517252.1:p.Ala266=
XM_011518948.2:c.1041T>A	XP_011517250.1:p.Ala347=
XM_011518949.2:c.1029T>A	XP_011517251.1:p.Ala343=
XM_011518950.2:c.798T>A	XP_011517252.1:p.Ala266=
XM_017015063.1:c.1041T>A	XP_016870552.1:p.Ala347=
XM_024447658.1:c.1029T>A	XP_024303426.1:p.Ala343=
NM_004612.4:c.1236T>A MANE Select	NP_004603.1:p.Ala412=
NM_001130916.3:c.1005T>A	NP_001124388.1:p.Ala335=
NM_001306210.2:c.1248T>A	NP_001293139.1:p.Ala416=