Canonical Allele Identifier: CA374233135

Gene: TGFBR1

Linked Data

• ClinVar Variation Id: 2683055
• ClinVar RCV Id: RCV003481922
• MyVariant Identifiers: chr9:g.101908873C>G (hg19) ; chr9:g.99146591C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146591C>G , CM000671.2:g.99146591C>G	GRCh38
NC_000009.11:g.101908873C>G , CM000671.1:g.101908873C>G	GRCh37
NC_000009.10:g.100948694C>G	NCBI36
NG_007461.1:g.46462C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.1030C>G	ENSP00000449934.2:p.Arg344Gly
ENST00000552573.7:c.1042C>G	ENSP00000447182.3:p.Arg348Gly
ENST00000548365.6:c.*159C>G	ENSP00000448518.2:n.*159C>G
ENST00000549021.6:c.799C>G	ENSP00000449028.2:p.Arg267Gly
ENST00000698941.1:c.1042C>G	ENSP00000514048.1:p.Arg348Gly
ENST00000698942.1:c.*1033C>G	ENSP00000514049.1:n.*1033C>G
ENST00000374994.9:c.1237C>G MANE Select	ENSP00000364133.4:p.Arg413Gly
ENST00000374990.6:c.1006C>G	ENSP00000364129.2:p.Arg336Gly
ENST00000374994.8:c.1237C>G	ENSP00000364133.4:p.Arg413Gly
ENST00000549766.5:c.1143-1063C>G	ENSP00000446685.1:n.1143-1063C>G
ENST00000550253.1:c.1030C>G	ENSP00000450052.1:p.Arg344Gly
ENST00000552516.5:c.1249C>G	ENSP00000447297.1:p.Arg417Gly
NM_001130916.1:c.1006C>G	NP_001124388.1:p.Arg336Gly
NM_001130916.2:c.1006C>G	NP_001124388.1:p.Arg336Gly
NM_001306210.1:c.1249C>G	NP_001293139.1:p.Arg417Gly
NM_004612.2:c.1237C>G	NP_004603.1:p.Arg413Gly
NM_004612.3:c.1237C>G	NP_004603.1:p.Arg413Gly
XM_011518948.1:c.1042C>G	XP_011517250.1:p.Arg348Gly
XM_011518949.1:c.1030C>G	XP_011517251.1:p.Arg344Gly
XM_011518950.1:c.799C>G	XP_011517252.1:p.Arg267Gly
XM_011518948.2:c.1042C>G	XP_011517250.1:p.Arg348Gly
XM_011518949.2:c.1030C>G	XP_011517251.1:p.Arg344Gly
XM_011518950.2:c.799C>G	XP_011517252.1:p.Arg267Gly
XM_017015063.1:c.1042C>G	XP_016870552.1:p.Arg348Gly
XM_024447658.1:c.1030C>G	XP_024303426.1:p.Arg344Gly
NM_004612.4:c.1237C>G MANE Select	NP_004603.1:p.Arg413Gly
NM_001130916.3:c.1006C>G	NP_001124388.1:p.Arg336Gly
NM_001306210.2:c.1249C>G	NP_001293139.1:p.Arg417Gly