Canonical Allele Identifier: CA1127252106
Gene: TGFBR1 HGNC NCBI

Linked Data

dbSNP Id: rs1827639439

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99142322_99142326del , CM000671.2:g.99142322_99142326del GRCh38
NC_000009.11:g.101904604_101904608del , CM000671.1:g.101904604_101904608del GRCh37
NC_000009.10:g.100944425_100944429del NCBI36
NG_007461.1:g.42193_42197del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547314.6:c.599-214_599-210del ENSP00000449934.2:n.599-214_599-210del
ENST00000552573.7:c.611-214_611-210del ENSP00000447182.3:n.611-214_611-210del
ENST00000548365.6:c.380-214_380-210del ENSP00000448518.2:n.380-214_380-210del
ENST00000549021.6:c.368-214_368-210del ENSP00000449028.2:n.368-214_368-210del
ENST00000698941.1:c.611-214_611-210del ENSP00000514048.1:n.611-214_611-210del
ENST00000698942.1:c.*602-214_*602-210del ENSP00000514049.1:n.*602-214_*602-210del
ENST00000374994.9:c.806-214_806-210del MANE Select ENSP00000364133.4:n.806-214_806-210del
ENST00000374990.6:c.575-214_575-210del ENSP00000364129.2:n.575-214_575-210del
ENST00000374994.8:c.806-214_806-210del ENSP00000364133.4:n.806-214_806-210del
ENST00000549766.5:c.818-214_818-210del ENSP00000446685.1:n.818-214_818-210del
ENST00000550253.1:c.599-214_599-210del ENSP00000450052.1:n.599-214_599-210del
ENST00000552516.5:c.818-214_818-210del ENSP00000447297.1:n.818-214_818-210del
NM_001130916.1:c.575-214_575-210del NP_001124388.1:n.575-214_575-210del
NM_001130916.2:c.575-214_575-210del NP_001124388.1:n.575-214_575-210del
NM_001306210.1:c.818-214_818-210del NP_001293139.1:n.818-214_818-210del
NM_004612.2:c.806-214_806-210del NP_004603.1:n.806-214_806-210del
NM_004612.3:c.806-214_806-210del NP_004603.1:n.806-214_806-210del
XM_011518948.1:c.611-214_611-210del XP_011517250.1:n.611-214_611-210del
XM_011518949.1:c.599-214_599-210del XP_011517251.1:n.599-214_599-210del
XM_011518950.1:c.368-214_368-210del XP_011517252.1:n.368-214_368-210del
XM_011518948.2:c.611-214_611-210del XP_011517250.1:n.611-214_611-210del
XM_011518949.2:c.599-214_599-210del XP_011517251.1:n.599-214_599-210del
XM_011518950.2:c.368-214_368-210del XP_011517252.1:n.368-214_368-210del
XM_017015063.1:c.611-214_611-210del XP_016870552.1:n.611-214_611-210del
XM_024447658.1:c.599-214_599-210del XP_024303426.1:n.599-214_599-210del
NM_004612.4:c.806-214_806-210del MANE Select NP_004603.1:n.806-214_806-210del
NM_001130916.3:c.575-214_575-210del NP_001124388.1:n.575-214_575-210del
NM_001306210.2:c.818-214_818-210del NP_001293139.1:n.818-214_818-210del