Canonical Allele Identifier: CA1867255846
Gene: TGFBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99137991C= , CM000671.2:g.99137991C= GRCh38
NC_000009.11:g.101900273C= , CM000671.1:g.101900273C= GRCh37
NC_000009.10:g.100940094C= NCBI36
NG_007461.1:g.37862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547314.6:c.500C= ENSP00000449934.2:p.Ser167=
ENST00000552573.7:c.512C= ENSP00000447182.3:p.Ser171=
ENST00000548365.6:c.380-4545C= ENSP00000448518.2:n.380-4545C=
ENST00000549021.6:c.269C= ENSP00000449028.2:p.Ser90=
ENST00000698941.1:c.512C= ENSP00000514048.1:p.Ser171=
ENST00000698942.1:c.*503C= ENSP00000514049.1:n.*503C=
ENST00000374994.9:c.707C= MANE Select ENSP00000364133.4:p.Ser236=
ENST00000374990.6:c.476C= ENSP00000364129.2:p.Ser159=
ENST00000374994.8:c.707C= ENSP00000364133.4:p.Ser236=
ENST00000549021.5:c.269C= ENSP00000449028.1:p.Ser90=
ENST00000549766.5:c.719C= ENSP00000446685.1:p.Ser240=
ENST00000550253.1:c.500C= ENSP00000450052.1:p.Ser167=
ENST00000552516.5:c.719C= ENSP00000447297.1:p.Ser240=
NM_001130916.1:c.476C= NP_001124388.1:p.Ser159=
NM_001130916.2:c.476C= NP_001124388.1:p.Ser159=
NM_001306210.1:c.719C= NP_001293139.1:p.Ser240=
NM_004612.2:c.707C= NP_004603.1:p.Ser236=
NM_004612.3:c.707C= NP_004603.1:p.Ser236=
XM_011518948.1:c.512C= XP_011517250.1:p.Ser171=
XM_011518949.1:c.500C= XP_011517251.1:p.Ser167=
XM_011518950.1:c.269C= XP_011517252.1:p.Ser90=
XM_011518948.2:c.512C= XP_011517250.1:p.Ser171=
XM_011518949.2:c.500C= XP_011517251.1:p.Ser167=
XM_011518950.2:c.269C= XP_011517252.1:p.Ser90=
XM_017015063.1:c.512C= XP_016870552.1:p.Ser171=
XM_024447658.1:c.500C= XP_024303426.1:p.Ser167=
NM_004612.4:c.707C= MANE Select NP_004603.1:p.Ser236=
NM_001130916.3:c.476C= NP_001124388.1:p.Ser159=
NM_001306210.2:c.719C= NP_001293139.1:p.Ser240=