Canonical Allele Identifier: CA1867260066
Gene: TGFBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99142599_99142603delinsATTAC , CM000671.2:g.99142599_99142603delinsATTAC GRCh38
NC_000009.11:g.101904881_101904885delinsATTAC , CM000671.1:g.101904881_101904885delinsATTAC GRCh37
NC_000009.10:g.100944702_100944706delinsATTAC NCBI36
NG_007461.1:g.42470_42474delinsATTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000547314.6:c.662_666delinsATTAC ENSP00000449934.2:p.Asp221=
ENST00000552573.7:c.674_678delinsATTAC ENSP00000447182.3:p.Asp225=
ENST00000548365.6:c.443_447delinsATTAC ENSP00000448518.2:p.Asp148=
ENST00000549021.6:c.431_435delinsATTAC ENSP00000449028.2:p.Asp144=
ENST00000698941.1:c.674_678delinsATTAC ENSP00000514048.1:p.Asp225=
ENST00000698942.1:c.*665_*669delinsATTAC ENSP00000514049.1:n.*665_*669delinsATTAC
ENST00000374994.9:c.869_873delinsATTAC MANE Select ENSP00000364133.4:p.Asp290=
ENST00000374990.6:c.638_642delinsATTAC ENSP00000364129.2:p.Asp213=
ENST00000374994.8:c.869_873delinsATTAC ENSP00000364133.4:p.Asp290=
ENST00000549766.5:c.881_885delinsATTAC ENSP00000446685.1:p.Asp294=
ENST00000550253.1:c.662_666delinsATTAC ENSP00000450052.1:p.Asp221=
ENST00000552516.5:c.881_885delinsATTAC ENSP00000447297.1:p.Asp294=
NM_001130916.1:c.638_642delinsATTAC NP_001124388.1:p.Asp213=
NM_001130916.2:c.638_642delinsATTAC NP_001124388.1:p.Asp213=
NM_001306210.1:c.881_885delinsATTAC NP_001293139.1:p.Asp294=
NM_004612.2:c.869_873delinsATTAC NP_004603.1:p.Asp290=
NM_004612.3:c.869_873delinsATTAC NP_004603.1:p.Asp290=
XM_011518948.1:c.674_678delinsATTAC XP_011517250.1:p.Asp225=
XM_011518949.1:c.662_666delinsATTAC XP_011517251.1:p.Asp221=
XM_011518950.1:c.431_435delinsATTAC XP_011517252.1:p.Asp144=
XM_011518948.2:c.674_678delinsATTAC XP_011517250.1:p.Asp225=
XM_011518949.2:c.662_666delinsATTAC XP_011517251.1:p.Asp221=
XM_011518950.2:c.431_435delinsATTAC XP_011517252.1:p.Asp144=
XM_017015063.1:c.674_678delinsATTAC XP_016870552.1:p.Asp225=
XM_024447658.1:c.662_666delinsATTAC XP_024303426.1:p.Asp221=
NM_004612.4:c.869_873delinsATTAC MANE Select NP_004603.1:p.Asp290=
NM_001130916.3:c.638_642delinsATTAC NP_001124388.1:p.Asp213=
NM_001306210.2:c.881_885delinsATTAC NP_001293139.1:p.Asp294=