Canonical Allele Identifier: CA008835

Gene: TGFBR1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99137883C>T , CM000671.2:g.99137883C>T	GRCh38
NC_000009.11:g.101900165C>T , CM000671.1:g.101900165C>T	GRCh37
NC_000009.10:g.100939986C>T	NCBI36
NG_007461.1:g.37754C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.392C>T	ENSP00000449934.2:p.Thr131Ile
ENST00000552573.7:c.404C>T	ENSP00000447182.3:p.Thr135Ile
ENST00000548365.6:c.380-4653C>T	ENSP00000448518.2:n.380-4653C>T
ENST00000549021.6:c.161C>T	ENSP00000449028.2:p.Thr54Ile
ENST00000698941.1:c.404C>T	ENSP00000514048.1:p.Thr135Ile
ENST00000698942.1:c.*395C>T	ENSP00000514049.1:n.*395C>T
ENST00000374994.9:c.599C>T MANE Select	ENSP00000364133.4:p.Thr200Ile
ENST00000374990.6:c.368C>T	ENSP00000364129.2:p.Thr123Ile
ENST00000374994.8:c.599C>T	ENSP00000364133.4:p.Thr200Ile
ENST00000549021.5:c.161C>T	ENSP00000449028.1:p.Thr54Ile
ENST00000549766.5:c.611C>T	ENSP00000446685.1:p.Thr204Ile
ENST00000550253.1:c.392C>T	ENSP00000450052.1:p.Thr131Ile
ENST00000552516.5:c.611C>T	ENSP00000447297.1:p.Thr204Ile
NM_001130916.1:c.368C>T	NP_001124388.1:p.Thr123Ile
NM_001130916.2:c.368C>T	NP_001124388.1:p.Thr123Ile
NM_001306210.1:c.611C>T	NP_001293139.1:p.Thr204Ile
NM_004612.2:c.599C>T	NP_004603.1:p.Thr200Ile
NM_004612.3:c.599C>T	NP_004603.1:p.Thr200Ile
XM_011518948.1:c.404C>T	XP_011517250.1:p.Thr135Ile
XM_011518949.1:c.392C>T	XP_011517251.1:p.Thr131Ile
XM_011518950.1:c.161C>T	XP_011517252.1:p.Thr54Ile
XM_011518948.2:c.404C>T	XP_011517250.1:p.Thr135Ile
XM_011518949.2:c.392C>T	XP_011517251.1:p.Thr131Ile
XM_011518950.2:c.161C>T	XP_011517252.1:p.Thr54Ile
XM_017015063.1:c.404C>T	XP_016870552.1:p.Thr135Ile
XM_024447658.1:c.392C>T	XP_024303426.1:p.Thr131Ile
NM_004612.4:c.599C>T MANE Select	NP_004603.1:p.Thr200Ile
NM_001130916.3:c.368C>T	NP_001124388.1:p.Thr123Ile
NM_001306210.2:c.611C>T	NP_001293139.1:p.Thr204Ile