Canonical Allele Identifier: CA466434487

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101904909G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142627G>T , CM000671.2:g.99142627G>T	GRCh38
NC_000009.11:g.101904909G>T , CM000671.1:g.101904909G>T	GRCh37
NC_000009.10:g.100944730G>T	NCBI36
NG_007461.1:g.42498G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.690G>T	ENSP00000449934.2:p.Val230=
ENST00000552573.7:c.702G>T	ENSP00000447182.3:p.Val234=
ENST00000548365.6:c.471G>T	ENSP00000448518.2:p.Val157=
ENST00000549021.6:c.459G>T	ENSP00000449028.2:p.Val153=
ENST00000698941.1:c.702G>T	ENSP00000514048.1:p.Val234=
ENST00000698942.1:c.*693G>T	ENSP00000514049.1:n.*693G>T
ENST00000374994.9:c.897G>T MANE Select	ENSP00000364133.4:p.Val299=
ENST00000374990.6:c.666G>T	ENSP00000364129.2:p.Val222=
ENST00000374994.8:c.897G>T	ENSP00000364133.4:p.Val299=
ENST00000549766.5:c.909G>T	ENSP00000446685.1:p.Val303=
ENST00000550253.1:c.690G>T	ENSP00000450052.1:p.Val230=
ENST00000552516.5:c.909G>T	ENSP00000447297.1:p.Val303=
NM_001130916.1:c.666G>T	NP_001124388.1:p.Val222=
NM_001130916.2:c.666G>T	NP_001124388.1:p.Val222=
NM_001306210.1:c.909G>T	NP_001293139.1:p.Val303=
NM_004612.2:c.897G>T	NP_004603.1:p.Val299=
NM_004612.3:c.897G>T	NP_004603.1:p.Val299=
XM_011518948.1:c.702G>T	XP_011517250.1:p.Val234=
XM_011518949.1:c.690G>T	XP_011517251.1:p.Val230=
XM_011518950.1:c.459G>T	XP_011517252.1:p.Val153=
XM_011518948.2:c.702G>T	XP_011517250.1:p.Val234=
XM_011518949.2:c.690G>T	XP_011517251.1:p.Val230=
XM_011518950.2:c.459G>T	XP_011517252.1:p.Val153=
XM_017015063.1:c.702G>T	XP_016870552.1:p.Val234=
XM_024447658.1:c.690G>T	XP_024303426.1:p.Val230=
NM_004612.4:c.897G>T MANE Select	NP_004603.1:p.Val299=
NM_001130916.3:c.666G>T	NP_001124388.1:p.Val222=
NM_001306210.2:c.909G>T	NP_001293139.1:p.Val303=