Canonical Allele Identifier: CA374232961

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908837A>G (hg19) ; chr9:g.99146555A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146555A>G , CM000671.2:g.99146555A>G	GRCh38
NC_000009.11:g.101908837A>G , CM000671.1:g.101908837A>G	GRCh37
NC_000009.10:g.100948658A>G	NCBI36
NG_007461.1:g.46426A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.994A>G	ENSP00000449934.2:p.Ile332Val
ENST00000552573.7:c.1006A>G	ENSP00000447182.3:p.Ile336Val
ENST00000548365.6:c.*123A>G	ENSP00000448518.2:n.*123A>G
ENST00000549021.6:c.763A>G	ENSP00000449028.2:p.Ile255Val
ENST00000698941.1:c.1006A>G	ENSP00000514048.1:p.Ile336Val
ENST00000698942.1:c.*997A>G	ENSP00000514049.1:n.*997A>G
ENST00000374994.9:c.1201A>G MANE Select	ENSP00000364133.4:p.Ile401Val
ENST00000374990.6:c.970A>G	ENSP00000364129.2:p.Ile324Val
ENST00000374994.8:c.1201A>G	ENSP00000364133.4:p.Ile401Val
ENST00000549766.5:c.1143-1099A>G	ENSP00000446685.1:n.1143-1099A>G
ENST00000550253.1:c.994A>G	ENSP00000450052.1:p.Ile332Val
ENST00000552516.5:c.1213A>G	ENSP00000447297.1:p.Ile405Val
NM_001130916.1:c.970A>G	NP_001124388.1:p.Ile324Val
NM_001130916.2:c.970A>G	NP_001124388.1:p.Ile324Val
NM_001306210.1:c.1213A>G	NP_001293139.1:p.Ile405Val
NM_004612.2:c.1201A>G	NP_004603.1:p.Ile401Val
NM_004612.3:c.1201A>G	NP_004603.1:p.Ile401Val
XM_011518948.1:c.1006A>G	XP_011517250.1:p.Ile336Val
XM_011518949.1:c.994A>G	XP_011517251.1:p.Ile332Val
XM_011518950.1:c.763A>G	XP_011517252.1:p.Ile255Val
XM_011518948.2:c.1006A>G	XP_011517250.1:p.Ile336Val
XM_011518949.2:c.994A>G	XP_011517251.1:p.Ile332Val
XM_011518950.2:c.763A>G	XP_011517252.1:p.Ile255Val
XM_017015063.1:c.1006A>G	XP_016870552.1:p.Ile336Val
XM_024447658.1:c.994A>G	XP_024303426.1:p.Ile332Val
NM_004612.4:c.1201A>G MANE Select	NP_004603.1:p.Ile401Val
NM_001130916.3:c.970A>G	NP_001124388.1:p.Ile324Val
NM_001306210.2:c.1213A>G	NP_001293139.1:p.Ile405Val