Canonical Allele Identifier: CA043820

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99144823A>C , CM000671.2:g.99144823A>C	GRCh38
NC_000009.11:g.101907105A>C , CM000671.1:g.101907105A>C	GRCh37
NC_000009.10:g.100946926A>C	NCBI36
NG_007461.1:g.44694A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004612.4:c.1065A>C MANE Select	NP_004603.1:p.Ala355=
ENST00000374994.9:c.1065A>C MANE Select	ENSP00000364133.4:p.Ala355=
NM_001130916.1:c.834A>C	NP_001124388.1:p.Ala278=
NM_001130916.2:c.834A>C	NP_001124388.1:p.Ala278=
NM_001130916.3:c.834A>C	NP_001124388.1:p.Ala278=
NM_001306210.1:c.1077A>C	NP_001293139.1:p.Ala359=
NM_001306210.2:c.1077A>C	NP_001293139.1:p.Ala359=
NM_004612.2:c.1065A>C	NP_004603.1:p.Ala355=
NM_004612.3:c.1065A>C	NP_004603.1:p.Ala355=
ENST00000374990.6:c.834A>C	ENSP00000364129.2:p.Ala278=
ENST00000374994.8:c.1065A>C	ENSP00000364133.4:p.Ala355=
ENST00000547314.6:c.858A>C	ENSP00000449934.2:p.Ala286=
ENST00000548365.6:c.639A>C	ENSP00000448518.2:p.Ala213=
ENST00000549021.6:c.627A>C	ENSP00000449028.2:p.Ala209=
ENST00000549766.5:c.1077A>C	ENSP00000446685.1:p.Ala359=
ENST00000550253.1:c.858A>C	ENSP00000450052.1:p.Ala286=
ENST00000552516.5:c.1077A>C	ENSP00000447297.1:p.Ala359=
ENST00000552573.7:c.870A>C	ENSP00000447182.3:p.Ala290=
ENST00000698941.1:c.870A>C	ENSP00000514048.1:p.Ala290=
ENST00000698942.1:c.*861A>C	ENSP00000514049.1:n.*861A>C
XM_011518948.1:c.870A>C	XP_011517250.1:p.Ala290=
XM_011518948.2:c.870A>C	XP_011517250.1:p.Ala290=
XM_011518949.1:c.858A>C	XP_011517251.1:p.Ala286=
XM_011518949.2:c.858A>C	XP_011517251.1:p.Ala286=
XM_011518950.1:c.627A>C	XP_011517252.1:p.Ala209=
XM_011518950.2:c.627A>C	XP_011517252.1:p.Ala209=
XM_017015063.1:c.870A>C	XP_016870552.1:p.Ala290=
XM_024447658.1:c.858A>C	XP_024303426.1:p.Ala286=