Canonical Allele Identifier: CA374229429

Gene: TGFBR1

Linked Data

• dbSNP Id: rs200018073
• MyVariant Identifiers: chr9:g.101900179A>T (hg19) ; chr9:g.99137897A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99137897A>T , CM000671.2:g.99137897A>T	GRCh38
NC_000009.11:g.101900179A>T , CM000671.1:g.101900179A>T	GRCh37
NC_000009.10:g.100940000A>T	NCBI36
NG_007461.1:g.37768A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.406A>T	ENSP00000449934.2:p.Ile136Phe
ENST00000552573.7:c.418A>T	ENSP00000447182.3:p.Ile140Phe
ENST00000548365.6:c.380-4639A>T	ENSP00000448518.2:n.380-4639A>T
ENST00000549021.6:c.175A>T	ENSP00000449028.2:p.Ile59Phe
ENST00000698941.1:c.418A>T	ENSP00000514048.1:p.Ile140Phe
ENST00000698942.1:c.*409A>T	ENSP00000514049.1:n.*409A>T
ENST00000374994.9:c.613A>T MANE Select	ENSP00000364133.4:p.Ile205Phe
ENST00000374990.6:c.382A>T	ENSP00000364129.2:p.Ile128Phe
ENST00000374994.8:c.613A>T	ENSP00000364133.4:p.Ile205Phe
ENST00000549021.5:c.175A>T	ENSP00000449028.1:p.Ile59Phe
ENST00000549766.5:c.625A>T	ENSP00000446685.1:p.Ile209Phe
ENST00000550253.1:c.406A>T	ENSP00000450052.1:p.Ile136Phe
ENST00000552516.5:c.625A>T	ENSP00000447297.1:p.Ile209Phe
NM_001130916.1:c.382A>T	NP_001124388.1:p.Ile128Phe
NM_001130916.2:c.382A>T	NP_001124388.1:p.Ile128Phe
NM_001306210.1:c.625A>T	NP_001293139.1:p.Ile209Phe
NM_004612.2:c.613A>T	NP_004603.1:p.Ile205Phe
NM_004612.3:c.613A>T	NP_004603.1:p.Ile205Phe
XM_011518948.1:c.418A>T	XP_011517250.1:p.Ile140Phe
XM_011518949.1:c.406A>T	XP_011517251.1:p.Ile136Phe
XM_011518950.1:c.175A>T	XP_011517252.1:p.Ile59Phe
XM_011518948.2:c.418A>T	XP_011517250.1:p.Ile140Phe
XM_011518949.2:c.406A>T	XP_011517251.1:p.Ile136Phe
XM_011518950.2:c.175A>T	XP_011517252.1:p.Ile59Phe
XM_017015063.1:c.418A>T	XP_016870552.1:p.Ile140Phe
XM_024447658.1:c.406A>T	XP_024303426.1:p.Ile136Phe
NM_004612.4:c.613A>T MANE Select	NP_004603.1:p.Ile205Phe
NM_001130916.3:c.382A>T	NP_001124388.1:p.Ile128Phe
NM_001306210.2:c.625A>T	NP_001293139.1:p.Ile209Phe