Canonical Allele Identifier: CA374232741

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908795T>G (hg19) ; chr9:g.99146513T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146513T>G , CM000671.2:g.99146513T>G	GRCh38
NC_000009.11:g.101908795T>G , CM000671.1:g.101908795T>G	GRCh37
NC_000009.10:g.100948616T>G	NCBI36
NG_007461.1:g.46384T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.952T>G	ENSP00000449934.2:p.Ser318Ala
ENST00000552573.7:c.964T>G	ENSP00000447182.3:p.Ser322Ala
ENST00000548365.6:c.*81T>G	ENSP00000448518.2:n.*81T>G
ENST00000549021.6:c.721T>G	ENSP00000449028.2:p.Ser241Ala
ENST00000698941.1:c.964T>G	ENSP00000514048.1:p.Ser322Ala
ENST00000698942.1:c.*955T>G	ENSP00000514049.1:n.*955T>G
ENST00000374994.9:c.1159T>G MANE Select	ENSP00000364133.4:p.Ser387Ala
ENST00000374990.6:c.928T>G	ENSP00000364129.2:p.Ser310Ala
ENST00000374994.8:c.1159T>G	ENSP00000364133.4:p.Ser387Ala
ENST00000549766.5:c.1143-1141T>G	ENSP00000446685.1:n.1143-1141T>G
ENST00000550253.1:c.952T>G	ENSP00000450052.1:p.Ser318Ala
ENST00000552516.5:c.1171T>G	ENSP00000447297.1:p.Ser391Ala
NM_001130916.1:c.928T>G	NP_001124388.1:p.Ser310Ala
NM_001130916.2:c.928T>G	NP_001124388.1:p.Ser310Ala
NM_001306210.1:c.1171T>G	NP_001293139.1:p.Ser391Ala
NM_004612.2:c.1159T>G	NP_004603.1:p.Ser387Ala
NM_004612.3:c.1159T>G	NP_004603.1:p.Ser387Ala
XM_011518948.1:c.964T>G	XP_011517250.1:p.Ser322Ala
XM_011518949.1:c.952T>G	XP_011517251.1:p.Ser318Ala
XM_011518950.1:c.721T>G	XP_011517252.1:p.Ser241Ala
XM_011518948.2:c.964T>G	XP_011517250.1:p.Ser322Ala
XM_011518949.2:c.952T>G	XP_011517251.1:p.Ser318Ala
XM_011518950.2:c.721T>G	XP_011517252.1:p.Ser241Ala
XM_017015063.1:c.964T>G	XP_016870552.1:p.Ser322Ala
XM_024447658.1:c.952T>G	XP_024303426.1:p.Ser318Ala
NM_004612.4:c.1159T>G MANE Select	NP_004603.1:p.Ser387Ala
NM_001130916.3:c.928T>G	NP_001124388.1:p.Ser310Ala
NM_001306210.2:c.1171T>G	NP_001293139.1:p.Ser391Ala