Canonical Allele Identifier: CA374228164

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101894923C>G (hg19) ; chr9:g.99132641C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99132641C>G , CM000671.2:g.99132641C>G	GRCh38
NC_000009.11:g.101894923C>G , CM000671.1:g.101894923C>G	GRCh37
NC_000009.10:g.100934744C>G	NCBI36
NG_007461.1:g.32512C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.269C>G	ENSP00000449934.2:p.Pro90Arg
ENST00000552573.7:c.281C>G	ENSP00000447182.3:p.Pro94Arg
ENST00000548365.6:c.281C>G	ENSP00000448518.2:p.Pro94Arg
ENST00000549021.6:c.136+3541C>G	ENSP00000449028.2:n.136+3541C>G
ENST00000698941.1:c.281C>G	ENSP00000514048.1:p.Pro94Arg
ENST00000698942.1:c.*272C>G	ENSP00000514049.1:n.*272C>G
ENST00000374994.9:c.476C>G MANE Select	ENSP00000364133.4:p.Pro159Arg
ENST00000374990.6:c.343+3541C>G	ENSP00000364129.2:n.343+3541C>G
ENST00000374994.8:c.476C>G	ENSP00000364133.4:p.Pro159Arg
ENST00000546584.1:c.269C>G	ENSP00000447707.2:p.Pro90Arg
ENST00000547314.5:c.269C>G	ENSP00000449934.1:p.Pro90Arg
ENST00000548365.5:c.281C>G	ENSP00000448518.1:p.Pro94Arg
ENST00000549021.5:c.136+3541C>G	ENSP00000449028.1:n.136+3541C>G
ENST00000549766.5:c.488C>G	ENSP00000446685.1:p.Pro163Arg
ENST00000550253.1:c.269C>G	ENSP00000450052.1:p.Pro90Arg
ENST00000552516.5:c.488C>G	ENSP00000447297.1:p.Pro163Arg
ENST00000552573.6:c.281C>G	ENSP00000447182.2:p.Pro94Arg
NM_001130916.1:c.343+3541C>G	NP_001124388.1:n.343+3541C>G
NM_001130916.2:c.343+3541C>G	NP_001124388.1:n.343+3541C>G
NM_001306210.1:c.488C>G	NP_001293139.1:p.Pro163Arg
NM_004612.2:c.476C>G	NP_004603.1:p.Pro159Arg
NM_004612.3:c.476C>G	NP_004603.1:p.Pro159Arg
XM_011518948.1:c.281C>G	XP_011517250.1:p.Pro94Arg
XM_011518949.1:c.269C>G	XP_011517251.1:p.Pro90Arg
XM_011518950.1:c.136+3541C>G	XP_011517252.1:n.136+3541C>G
XM_011518948.2:c.281C>G	XP_011517250.1:p.Pro94Arg
XM_011518949.2:c.269C>G	XP_011517251.1:p.Pro90Arg
XM_011518950.2:c.136+3541C>G	XP_011517252.1:n.136+3541C>G
XM_017015063.1:c.281C>G	XP_016870552.1:p.Pro94Arg
XM_024447658.1:c.269C>G	XP_024303426.1:p.Pro90Arg
NM_004612.4:c.476C>G MANE Select	NP_004603.1:p.Pro159Arg
NM_001130916.3:c.343+3541C>G	NP_001124388.1:n.343+3541C>G
NM_001306210.2:c.488C>G	NP_001293139.1:p.Pro163Arg