Canonical Allele Identifier: CA374232620

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908777C>A (hg19) ; chr9:g.99146495C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146495C>A , CM000671.2:g.99146495C>A	GRCh38
NC_000009.11:g.101908777C>A , CM000671.1:g.101908777C>A	GRCh37
NC_000009.10:g.100948598C>A	NCBI36
NG_007461.1:g.46366C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.934C>A	ENSP00000449934.2:p.Pro312Thr
ENST00000552573.7:c.946C>A	ENSP00000447182.3:p.Pro316Thr
ENST00000548365.6:c.*63C>A	ENSP00000448518.2:n.*63C>A
ENST00000549021.6:c.703C>A	ENSP00000449028.2:p.Pro235Thr
ENST00000698941.1:c.946C>A	ENSP00000514048.1:p.Pro316Thr
ENST00000698942.1:c.*937C>A	ENSP00000514049.1:n.*937C>A
ENST00000374994.9:c.1141C>A MANE Select	ENSP00000364133.4:p.Pro381Thr
ENST00000374990.6:c.910C>A	ENSP00000364129.2:p.Pro304Thr
ENST00000374994.8:c.1141C>A	ENSP00000364133.4:p.Pro381Thr
ENST00000549766.5:c.1143-1159C>A	ENSP00000446685.1:n.1143-1159C>A
ENST00000550253.1:c.934C>A	ENSP00000450052.1:p.Pro312Thr
ENST00000552516.5:c.1153C>A	ENSP00000447297.1:p.Pro385Thr
NM_001130916.1:c.910C>A	NP_001124388.1:p.Pro304Thr
NM_001130916.2:c.910C>A	NP_001124388.1:p.Pro304Thr
NM_001306210.1:c.1153C>A	NP_001293139.1:p.Pro385Thr
NM_004612.2:c.1141C>A	NP_004603.1:p.Pro381Thr
NM_004612.3:c.1141C>A	NP_004603.1:p.Pro381Thr
XM_011518948.1:c.946C>A	XP_011517250.1:p.Pro316Thr
XM_011518949.1:c.934C>A	XP_011517251.1:p.Pro312Thr
XM_011518950.1:c.703C>A	XP_011517252.1:p.Pro235Thr
XM_011518948.2:c.946C>A	XP_011517250.1:p.Pro316Thr
XM_011518949.2:c.934C>A	XP_011517251.1:p.Pro312Thr
XM_011518950.2:c.703C>A	XP_011517252.1:p.Pro235Thr
XM_017015063.1:c.946C>A	XP_016870552.1:p.Pro316Thr
XM_024447658.1:c.934C>A	XP_024303426.1:p.Pro312Thr
NM_004612.4:c.1141C>A MANE Select	NP_004603.1:p.Pro381Thr
NM_001130916.3:c.910C>A	NP_001124388.1:p.Pro304Thr
NM_001306210.2:c.1153C>A	NP_001293139.1:p.Pro385Thr