Canonical Allele Identifier: CA466435377

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101908845A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99146563A>T , CM000671.2:g.99146563A>T	GRCh38
NC_000009.11:g.101908845A>T , CM000671.1:g.101908845A>T	GRCh37
NC_000009.10:g.100948666A>T	NCBI36
NG_007461.1:g.46434A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.1002A>T	ENSP00000449934.2:p.Ala334=
ENST00000552573.7:c.1014A>T	ENSP00000447182.3:p.Ala338=
ENST00000548365.6:c.*131A>T	ENSP00000448518.2:n.*131A>T
ENST00000549021.6:c.771A>T	ENSP00000449028.2:p.Ala257=
ENST00000698941.1:c.1014A>T	ENSP00000514048.1:p.Ala338=
ENST00000698942.1:c.*1005A>T	ENSP00000514049.1:n.*1005A>T
ENST00000374994.9:c.1209A>T MANE Select	ENSP00000364133.4:p.Ala403=
ENST00000374990.6:c.978A>T	ENSP00000364129.2:p.Ala326=
ENST00000374994.8:c.1209A>T	ENSP00000364133.4:p.Ala403=
ENST00000549766.5:c.1143-1091A>T	ENSP00000446685.1:n.1143-1091A>T
ENST00000550253.1:c.1002A>T	ENSP00000450052.1:p.Ala334=
ENST00000552516.5:c.1221A>T	ENSP00000447297.1:p.Ala407=
NM_001130916.1:c.978A>T	NP_001124388.1:p.Ala326=
NM_001130916.2:c.978A>T	NP_001124388.1:p.Ala326=
NM_001306210.1:c.1221A>T	NP_001293139.1:p.Ala407=
NM_004612.2:c.1209A>T	NP_004603.1:p.Ala403=
NM_004612.3:c.1209A>T	NP_004603.1:p.Ala403=
XM_011518948.1:c.1014A>T	XP_011517250.1:p.Ala338=
XM_011518949.1:c.1002A>T	XP_011517251.1:p.Ala334=
XM_011518950.1:c.771A>T	XP_011517252.1:p.Ala257=
XM_011518948.2:c.1014A>T	XP_011517250.1:p.Ala338=
XM_011518949.2:c.1002A>T	XP_011517251.1:p.Ala334=
XM_011518950.2:c.771A>T	XP_011517252.1:p.Ala257=
XM_017015063.1:c.1014A>T	XP_016870552.1:p.Ala338=
XM_024447658.1:c.1002A>T	XP_024303426.1:p.Ala334=
NM_004612.4:c.1209A>T MANE Select	NP_004603.1:p.Ala403=
NM_001130916.3:c.978A>T	NP_001124388.1:p.Ala326=
NM_001306210.2:c.1221A>T	NP_001293139.1:p.Ala407=