Canonical Allele Identifier: CA466434453

Gene: TGFBR1

Linked Data

• gnomAD v4: 9-99142600-T-C
• MyVariant Identifiers: chr9:g.101904882T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99142600T>C , CM000671.2:g.99142600T>C	GRCh38
NC_000009.11:g.101904882T>C , CM000671.1:g.101904882T>C	GRCh37
NC_000009.10:g.100944703T>C	NCBI36
NG_007461.1:g.42471T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.663T>C	ENSP00000449934.2:p.Asp221=
ENST00000552573.7:c.675T>C	ENSP00000447182.3:p.Asp225=
ENST00000548365.6:c.444T>C	ENSP00000448518.2:p.Asp148=
ENST00000549021.6:c.432T>C	ENSP00000449028.2:p.Asp144=
ENST00000698941.1:c.675T>C	ENSP00000514048.1:p.Asp225=
ENST00000698942.1:c.*666T>C	ENSP00000514049.1:n.*666T>C
ENST00000374994.9:c.870T>C MANE Select	ENSP00000364133.4:p.Asp290=
ENST00000374990.6:c.639T>C	ENSP00000364129.2:p.Asp213=
ENST00000374994.8:c.870T>C	ENSP00000364133.4:p.Asp290=
ENST00000549766.5:c.882T>C	ENSP00000446685.1:p.Asp294=
ENST00000550253.1:c.663T>C	ENSP00000450052.1:p.Asp221=
ENST00000552516.5:c.882T>C	ENSP00000447297.1:p.Asp294=
NM_001130916.1:c.639T>C	NP_001124388.1:p.Asp213=
NM_001130916.2:c.639T>C	NP_001124388.1:p.Asp213=
NM_001306210.1:c.882T>C	NP_001293139.1:p.Asp294=
NM_004612.2:c.870T>C	NP_004603.1:p.Asp290=
NM_004612.3:c.870T>C	NP_004603.1:p.Asp290=
XM_011518948.1:c.675T>C	XP_011517250.1:p.Asp225=
XM_011518949.1:c.663T>C	XP_011517251.1:p.Asp221=
XM_011518950.1:c.432T>C	XP_011517252.1:p.Asp144=
XM_011518948.2:c.675T>C	XP_011517250.1:p.Asp225=
XM_011518949.2:c.663T>C	XP_011517251.1:p.Asp221=
XM_011518950.2:c.432T>C	XP_011517252.1:p.Asp144=
XM_017015063.1:c.675T>C	XP_016870552.1:p.Asp225=
XM_024447658.1:c.663T>C	XP_024303426.1:p.Asp221=
NM_004612.4:c.870T>C MANE Select	NP_004603.1:p.Asp290=
NM_001130916.3:c.639T>C	NP_001124388.1:p.Asp213=
NM_001306210.2:c.882T>C	NP_001293139.1:p.Asp294=