Canonical Allele Identifier: CA374230742

Gene: TGFBR1

Linked Data

• ClinVar Variation Id: 573117
• ClinVar RCV Id: RCV000694696
• dbSNP Id: rs1564168346
• MyVariant Identifiers: chr9:g.101904935C>T (hg19) ; chr9:g.99142653C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142653C>T , CM000671.2:g.99142653C>T	GRCh38
NC_000009.11:g.101904935C>T , CM000671.1:g.101904935C>T	GRCh37
NC_000009.10:g.100944756C>T	NCBI36
NG_007461.1:g.42524C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.716C>T	ENSP00000449934.2:p.Ser239Phe
ENST00000552573.7:c.728C>T	ENSP00000447182.3:p.Ser243Phe
ENST00000548365.6:c.497C>T	ENSP00000448518.2:p.Ser166Phe
ENST00000549021.6:c.485C>T	ENSP00000449028.2:p.Ser162Phe
ENST00000698941.1:c.728C>T	ENSP00000514048.1:p.Ser243Phe
ENST00000698942.1:c.*719C>T	ENSP00000514049.1:n.*719C>T
ENST00000374994.9:c.923C>T MANE Select	ENSP00000364133.4:p.Ser308Phe
ENST00000374990.6:c.692C>T	ENSP00000364129.2:p.Ser231Phe
ENST00000374994.8:c.923C>T	ENSP00000364133.4:p.Ser308Phe
ENST00000549766.5:c.935C>T	ENSP00000446685.1:p.Ser312Phe
ENST00000550253.1:c.716C>T	ENSP00000450052.1:p.Ser239Phe
ENST00000552516.5:c.935C>T	ENSP00000447297.1:p.Ser312Phe
NM_001130916.1:c.692C>T	NP_001124388.1:p.Ser231Phe
NM_001130916.2:c.692C>T	NP_001124388.1:p.Ser231Phe
NM_001306210.1:c.935C>T	NP_001293139.1:p.Ser312Phe
NM_004612.2:c.923C>T	NP_004603.1:p.Ser308Phe
NM_004612.3:c.923C>T	NP_004603.1:p.Ser308Phe
XM_011518948.1:c.728C>T	XP_011517250.1:p.Ser243Phe
XM_011518949.1:c.716C>T	XP_011517251.1:p.Ser239Phe
XM_011518950.1:c.485C>T	XP_011517252.1:p.Ser162Phe
XM_011518948.2:c.728C>T	XP_011517250.1:p.Ser243Phe
XM_011518949.2:c.716C>T	XP_011517251.1:p.Ser239Phe
XM_011518950.2:c.485C>T	XP_011517252.1:p.Ser162Phe
XM_017015063.1:c.728C>T	XP_016870552.1:p.Ser243Phe
XM_024447658.1:c.716C>T	XP_024303426.1:p.Ser239Phe
NM_004612.4:c.923C>T MANE Select	NP_004603.1:p.Ser308Phe
NM_001130916.3:c.692C>T	NP_001124388.1:p.Ser231Phe
NM_001306210.2:c.935C>T	NP_001293139.1:p.Ser312Phe