Canonical Allele Identifier: CA374230683

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101904908T>G (hg19) ; chr9:g.99142626T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142626T>G , CM000671.2:g.99142626T>G	GRCh38
NC_000009.11:g.101904908T>G , CM000671.1:g.101904908T>G	GRCh37
NC_000009.10:g.100944729T>G	NCBI36
NG_007461.1:g.42497T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.689T>G	ENSP00000449934.2:p.Val230Gly
ENST00000552573.7:c.701T>G	ENSP00000447182.3:p.Val234Gly
ENST00000548365.6:c.470T>G	ENSP00000448518.2:p.Val157Gly
ENST00000549021.6:c.458T>G	ENSP00000449028.2:p.Val153Gly
ENST00000698941.1:c.701T>G	ENSP00000514048.1:p.Val234Gly
ENST00000698942.1:c.*692T>G	ENSP00000514049.1:n.*692T>G
ENST00000374994.9:c.896T>G MANE Select	ENSP00000364133.4:p.Val299Gly
ENST00000374990.6:c.665T>G	ENSP00000364129.2:p.Val222Gly
ENST00000374994.8:c.896T>G	ENSP00000364133.4:p.Val299Gly
ENST00000549766.5:c.908T>G	ENSP00000446685.1:p.Val303Gly
ENST00000550253.1:c.689T>G	ENSP00000450052.1:p.Val230Gly
ENST00000552516.5:c.908T>G	ENSP00000447297.1:p.Val303Gly
NM_001130916.1:c.665T>G	NP_001124388.1:p.Val222Gly
NM_001130916.2:c.665T>G	NP_001124388.1:p.Val222Gly
NM_001306210.1:c.908T>G	NP_001293139.1:p.Val303Gly
NM_004612.2:c.896T>G	NP_004603.1:p.Val299Gly
NM_004612.3:c.896T>G	NP_004603.1:p.Val299Gly
XM_011518948.1:c.701T>G	XP_011517250.1:p.Val234Gly
XM_011518949.1:c.689T>G	XP_011517251.1:p.Val230Gly
XM_011518950.1:c.458T>G	XP_011517252.1:p.Val153Gly
XM_011518948.2:c.701T>G	XP_011517250.1:p.Val234Gly
XM_011518949.2:c.689T>G	XP_011517251.1:p.Val230Gly
XM_011518950.2:c.458T>G	XP_011517252.1:p.Val153Gly
XM_017015063.1:c.701T>G	XP_016870552.1:p.Val234Gly
XM_024447658.1:c.689T>G	XP_024303426.1:p.Val230Gly
NM_004612.4:c.896T>G MANE Select	NP_004603.1:p.Val299Gly
NM_001130916.3:c.665T>G	NP_001124388.1:p.Val222Gly
NM_001306210.2:c.908T>G	NP_001293139.1:p.Val303Gly