Canonical Allele Identifier: CA1867270671
Gene: TGFBR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99152001G= , CM000671.2:g.99152001G= GRCh38
NC_000009.11:g.101914283G= , CM000671.1:g.101914283G= GRCh37
NC_000009.10:g.100954104G= NCBI36
NG_007461.1:g.51872G=

Transcript Alleles

HGVS Amino-acid change
ENST00000547314.6:c.*2696G= ENSP00000449934.2:n.*2696G=
ENST00000552573.7:c.*2696G= ENSP00000447182.3:n.*2696G=
ENST00000374994.9:c.*2696G= MANE Select ENSP00000364133.4:n.*2696G=
ENST00000374990.6:c.*2696G= ENSP00000364129.2:n.*2696G=
ENST00000374994.8:c.*2696G= ENSP00000364133.4:n.*2696G=
ENST00000552516.5:c.*2696G= ENSP00000447297.1:n.*2696G=
NM_001130916.1:c.*2696G= NP_001124388.1:n.*2696G=
NM_001130916.2:c.*2696G= NP_001124388.1:n.*2696G=
NM_001306210.1:c.*2696G= NP_001293139.1:n.*2696G=
NM_004612.2:c.*2696G= NP_004603.1:n.*2696G=
NM_004612.3:c.*2696G= NP_004603.1:n.*2696G=
XM_011518948.1:c.*2696G= XP_011517250.1:n.*2696G=
XM_011518949.1:c.*2696G= XP_011517251.1:n.*2696G=
XM_011518950.1:c.*2696G= XP_011517252.1:n.*2696G=
NM_004612.4:c.*2696G= MANE Select NP_004603.1:n.*2696G=
NM_001130916.3:c.*2696G= NP_001124388.1:n.*2696G=
NM_001306210.2:c.*2696G= NP_001293139.1:n.*2696G=