Canonical Allele Identifier: CA1867274295
Gene: TGFBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99153703T= , CM000671.2:g.99153703T= GRCh38
NC_000009.11:g.101915985T= , CM000671.1:g.101915985T= GRCh37
NC_000009.10:g.100955806T= NCBI36
NG_007461.1:g.53574T=

Transcript Alleles

HGVS Amino-acid change
ENST00000547314.6:c.*4398T= ENSP00000449934.2:n.*4398T=
ENST00000552573.7:c.*4398T= ENSP00000447182.3:n.*4398T=
ENST00000374994.9:c.*4398T= MANE Select ENSP00000364133.4:n.*4398T=
ENST00000374994.8:c.*4398T= ENSP00000364133.4:n.*4398T=
NM_001130916.1:c.*4398T= NP_001124388.1:n.*4398T=
NM_001130916.2:c.*4398T= NP_001124388.1:n.*4398T=
NM_001306210.1:c.*4398T= NP_001293139.1:n.*4398T=
NM_004612.2:c.*4398T= NP_004603.1:n.*4398T=
NM_004612.3:c.*4398T= NP_004603.1:n.*4398T=
NM_004612.4:c.*4398T= MANE Select NP_004603.1:n.*4398T=
NM_001130916.3:c.*4398T= NP_001124388.1:n.*4398T=
NM_001306210.2:c.*4398T= NP_001293139.1:n.*4398T=