Canonical Allele Identifier: CA466435371

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908842T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146560T>C , CM000671.2:g.99146560T>C	GRCh38
NC_000009.11:g.101908842T>C , CM000671.1:g.101908842T>C	GRCh37
NC_000009.10:g.100948663T>C	NCBI36
NG_007461.1:g.46431T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.999T>C	ENSP00000449934.2:p.Tyr333=
ENST00000552573.7:c.1011T>C	ENSP00000447182.3:p.Tyr337=
ENST00000548365.6:c.*128T>C	ENSP00000448518.2:n.*128T>C
ENST00000549021.6:c.768T>C	ENSP00000449028.2:p.Tyr256=
ENST00000698941.1:c.1011T>C	ENSP00000514048.1:p.Tyr337=
ENST00000698942.1:c.*1002T>C	ENSP00000514049.1:n.*1002T>C
ENST00000374994.9:c.1206T>C MANE Select	ENSP00000364133.4:p.Tyr402=
ENST00000374990.6:c.975T>C	ENSP00000364129.2:p.Tyr325=
ENST00000374994.8:c.1206T>C	ENSP00000364133.4:p.Tyr402=
ENST00000549766.5:c.1143-1094T>C	ENSP00000446685.1:n.1143-1094T>C
ENST00000550253.1:c.999T>C	ENSP00000450052.1:p.Tyr333=
ENST00000552516.5:c.1218T>C	ENSP00000447297.1:p.Tyr406=
NM_001130916.1:c.975T>C	NP_001124388.1:p.Tyr325=
NM_001130916.2:c.975T>C	NP_001124388.1:p.Tyr325=
NM_001306210.1:c.1218T>C	NP_001293139.1:p.Tyr406=
NM_004612.2:c.1206T>C	NP_004603.1:p.Tyr402=
NM_004612.3:c.1206T>C	NP_004603.1:p.Tyr402=
XM_011518948.1:c.1011T>C	XP_011517250.1:p.Tyr337=
XM_011518949.1:c.999T>C	XP_011517251.1:p.Tyr333=
XM_011518950.1:c.768T>C	XP_011517252.1:p.Tyr256=
XM_011518948.2:c.1011T>C	XP_011517250.1:p.Tyr337=
XM_011518949.2:c.999T>C	XP_011517251.1:p.Tyr333=
XM_011518950.2:c.768T>C	XP_011517252.1:p.Tyr256=
XM_017015063.1:c.1011T>C	XP_016870552.1:p.Tyr337=
XM_024447658.1:c.999T>C	XP_024303426.1:p.Tyr333=
NM_004612.4:c.1206T>C MANE Select	NP_004603.1:p.Tyr402=
NM_001130916.3:c.975T>C	NP_001124388.1:p.Tyr325=
NM_001306210.2:c.1218T>C	NP_001293139.1:p.Tyr406=