Canonical Allele Identifier: CA374232595

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908773G>A (hg19) ; chr9:g.99146491G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146491G>A , CM000671.2:g.99146491G>A	GRCh38
NC_000009.11:g.101908773G>A , CM000671.1:g.101908773G>A	GRCh37
NC_000009.10:g.100948594G>A	NCBI36
NG_007461.1:g.46362G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.930G>A	ENSP00000449934.2:p.Met310Ile
ENST00000552573.7:c.942G>A	ENSP00000447182.3:p.Met314Ile
ENST00000548365.6:c.*59G>A	ENSP00000448518.2:n.*59G>A
ENST00000549021.6:c.699G>A	ENSP00000449028.2:p.Met233Ile
ENST00000698941.1:c.942G>A	ENSP00000514048.1:p.Met314Ile
ENST00000698942.1:c.*933G>A	ENSP00000514049.1:n.*933G>A
ENST00000374994.9:c.1137G>A MANE Select	ENSP00000364133.4:p.Met379Ile
ENST00000374990.6:c.906G>A	ENSP00000364129.2:p.Met302Ile
ENST00000374994.8:c.1137G>A	ENSP00000364133.4:p.Met379Ile
ENST00000549766.5:c.1143-1163G>A	ENSP00000446685.1:n.1143-1163G>A
ENST00000550253.1:c.930G>A	ENSP00000450052.1:p.Met310Ile
ENST00000552516.5:c.1149G>A	ENSP00000447297.1:p.Met383Ile
NM_001130916.1:c.906G>A	NP_001124388.1:p.Met302Ile
NM_001130916.2:c.906G>A	NP_001124388.1:p.Met302Ile
NM_001306210.1:c.1149G>A	NP_001293139.1:p.Met383Ile
NM_004612.2:c.1137G>A	NP_004603.1:p.Met379Ile
NM_004612.3:c.1137G>A	NP_004603.1:p.Met379Ile
XM_011518948.1:c.942G>A	XP_011517250.1:p.Met314Ile
XM_011518949.1:c.930G>A	XP_011517251.1:p.Met310Ile
XM_011518950.1:c.699G>A	XP_011517252.1:p.Met233Ile
XM_011518948.2:c.942G>A	XP_011517250.1:p.Met314Ile
XM_011518949.2:c.930G>A	XP_011517251.1:p.Met310Ile
XM_011518950.2:c.699G>A	XP_011517252.1:p.Met233Ile
XM_017015063.1:c.942G>A	XP_016870552.1:p.Met314Ile
XM_024447658.1:c.930G>A	XP_024303426.1:p.Met310Ile
NM_004612.4:c.1137G>A MANE Select	NP_004603.1:p.Met379Ile
NM_001130916.3:c.906G>A	NP_001124388.1:p.Met302Ile
NM_001306210.2:c.1149G>A	NP_001293139.1:p.Met383Ile