Canonical Allele Identifier: CA466434480

Gene: TGFBR1

Linked Data

• COSMIC: COSM1163519
• MyVariant Identifiers: chr9:g.101904903T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142621T>C , CM000671.2:g.99142621T>C	GRCh38
NC_000009.11:g.101904903T>C , CM000671.1:g.101904903T>C	GRCh37
NC_000009.10:g.100944724T>C	NCBI36
NG_007461.1:g.42492T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.684T>C	ENSP00000449934.2:p.Val228=
ENST00000552573.7:c.696T>C	ENSP00000447182.3:p.Val232=
ENST00000548365.6:c.465T>C	ENSP00000448518.2:p.Val155=
ENST00000549021.6:c.453T>C	ENSP00000449028.2:p.Val151=
ENST00000698941.1:c.696T>C	ENSP00000514048.1:p.Val232=
ENST00000698942.1:c.*687T>C	ENSP00000514049.1:n.*687T>C
ENST00000374994.9:c.891T>C MANE Select	ENSP00000364133.4:p.Val297=
ENST00000374990.6:c.660T>C	ENSP00000364129.2:p.Val220=
ENST00000374994.8:c.891T>C	ENSP00000364133.4:p.Val297=
ENST00000549766.5:c.903T>C	ENSP00000446685.1:p.Val301=
ENST00000550253.1:c.684T>C	ENSP00000450052.1:p.Val228=
ENST00000552516.5:c.903T>C	ENSP00000447297.1:p.Val301=
NM_001130916.1:c.660T>C	NP_001124388.1:p.Val220=
NM_001130916.2:c.660T>C	NP_001124388.1:p.Val220=
NM_001306210.1:c.903T>C	NP_001293139.1:p.Val301=
NM_004612.2:c.891T>C	NP_004603.1:p.Val297=
NM_004612.3:c.891T>C	NP_004603.1:p.Val297=
XM_011518948.1:c.696T>C	XP_011517250.1:p.Val232=
XM_011518949.1:c.684T>C	XP_011517251.1:p.Val228=
XM_011518950.1:c.453T>C	XP_011517252.1:p.Val151=
XM_011518948.2:c.696T>C	XP_011517250.1:p.Val232=
XM_011518949.2:c.684T>C	XP_011517251.1:p.Val228=
XM_011518950.2:c.453T>C	XP_011517252.1:p.Val151=
XM_017015063.1:c.696T>C	XP_016870552.1:p.Val232=
XM_024447658.1:c.684T>C	XP_024303426.1:p.Val228=
NM_004612.4:c.891T>C MANE Select	NP_004603.1:p.Val297=
NM_001130916.3:c.660T>C	NP_001124388.1:p.Val220=
NM_001306210.2:c.903T>C	NP_001293139.1:p.Val301=