Canonical Allele Identifier: CA374230604

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101904871T>A (hg19) ; chr9:g.99142589T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142589T>A , CM000671.2:g.99142589T>A	GRCh38
NC_000009.11:g.101904871T>A , CM000671.1:g.101904871T>A	GRCh37
NC_000009.10:g.100944692T>A	NCBI36
NG_007461.1:g.42460T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.652T>A	ENSP00000449934.2:p.Ser218Thr
ENST00000552573.7:c.664T>A	ENSP00000447182.3:p.Ser222Thr
ENST00000548365.6:c.433T>A	ENSP00000448518.2:p.Ser145Thr
ENST00000549021.6:c.421T>A	ENSP00000449028.2:p.Ser141Thr
ENST00000698941.1:c.664T>A	ENSP00000514048.1:p.Ser222Thr
ENST00000698942.1:c.*655T>A	ENSP00000514049.1:n.*655T>A
ENST00000374994.9:c.859T>A MANE Select	ENSP00000364133.4:p.Ser287Thr
ENST00000374990.6:c.628T>A	ENSP00000364129.2:p.Ser210Thr
ENST00000374994.8:c.859T>A	ENSP00000364133.4:p.Ser287Thr
ENST00000549766.5:c.871T>A	ENSP00000446685.1:p.Ser291Thr
ENST00000550253.1:c.652T>A	ENSP00000450052.1:p.Ser218Thr
ENST00000552516.5:c.871T>A	ENSP00000447297.1:p.Ser291Thr
NM_001130916.1:c.628T>A	NP_001124388.1:p.Ser210Thr
NM_001130916.2:c.628T>A	NP_001124388.1:p.Ser210Thr
NM_001306210.1:c.871T>A	NP_001293139.1:p.Ser291Thr
NM_004612.2:c.859T>A	NP_004603.1:p.Ser287Thr
NM_004612.3:c.859T>A	NP_004603.1:p.Ser287Thr
XM_011518948.1:c.664T>A	XP_011517250.1:p.Ser222Thr
XM_011518949.1:c.652T>A	XP_011517251.1:p.Ser218Thr
XM_011518950.1:c.421T>A	XP_011517252.1:p.Ser141Thr
XM_011518948.2:c.664T>A	XP_011517250.1:p.Ser222Thr
XM_011518949.2:c.652T>A	XP_011517251.1:p.Ser218Thr
XM_011518950.2:c.421T>A	XP_011517252.1:p.Ser141Thr
XM_017015063.1:c.664T>A	XP_016870552.1:p.Ser222Thr
XM_024447658.1:c.652T>A	XP_024303426.1:p.Ser218Thr
NM_004612.4:c.859T>A MANE Select	NP_004603.1:p.Ser287Thr
NM_001130916.3:c.628T>A	NP_001124388.1:p.Ser210Thr
NM_001306210.2:c.871T>A	NP_001293139.1:p.Ser291Thr