Canonical Allele Identifier: CA466434153

Gene: TGFBR1

Linked Data

• MyVariant Identifiers: chr9:g.101900178T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99137896T>C , CM000671.2:g.99137896T>C	GRCh38
NC_000009.11:g.101900178T>C , CM000671.1:g.101900178T>C	GRCh37
NC_000009.10:g.100939999T>C	NCBI36
NG_007461.1:g.37767T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.405T>C	ENSP00000449934.2:p.Thr135=
ENST00000552573.7:c.417T>C	ENSP00000447182.3:p.Thr139=
ENST00000548365.6:c.380-4640T>C	ENSP00000448518.2:n.380-4640T>C
ENST00000549021.6:c.174T>C	ENSP00000449028.2:p.Thr58=
ENST00000698941.1:c.417T>C	ENSP00000514048.1:p.Thr139=
ENST00000698942.1:c.*408T>C	ENSP00000514049.1:n.*408T>C
ENST00000374994.9:c.612T>C MANE Select	ENSP00000364133.4:p.Thr204=
ENST00000374990.6:c.381T>C	ENSP00000364129.2:p.Thr127=
ENST00000374994.8:c.612T>C	ENSP00000364133.4:p.Thr204=
ENST00000549021.5:c.174T>C	ENSP00000449028.1:p.Thr58=
ENST00000549766.5:c.624T>C	ENSP00000446685.1:p.Thr208=
ENST00000550253.1:c.405T>C	ENSP00000450052.1:p.Thr135=
ENST00000552516.5:c.624T>C	ENSP00000447297.1:p.Thr208=
NM_001130916.1:c.381T>C	NP_001124388.1:p.Thr127=
NM_001130916.2:c.381T>C	NP_001124388.1:p.Thr127=
NM_001306210.1:c.624T>C	NP_001293139.1:p.Thr208=
NM_004612.2:c.612T>C	NP_004603.1:p.Thr204=
NM_004612.3:c.612T>C	NP_004603.1:p.Thr204=
XM_011518948.1:c.417T>C	XP_011517250.1:p.Thr139=
XM_011518949.1:c.405T>C	XP_011517251.1:p.Thr135=
XM_011518950.1:c.174T>C	XP_011517252.1:p.Thr58=
XM_011518948.2:c.417T>C	XP_011517250.1:p.Thr139=
XM_011518949.2:c.405T>C	XP_011517251.1:p.Thr135=
XM_011518950.2:c.174T>C	XP_011517252.1:p.Thr58=
XM_017015063.1:c.417T>C	XP_016870552.1:p.Thr139=
XM_024447658.1:c.405T>C	XP_024303426.1:p.Thr135=
NM_004612.4:c.612T>C MANE Select	NP_004603.1:p.Thr204=
NM_001130916.3:c.381T>C	NP_001124388.1:p.Thr127=
NM_001306210.2:c.624T>C	NP_001293139.1:p.Thr208=