Canonical Allele Identifier: CA869145448
Gene: TGFBR1 HGNC NCBI

Linked Data

dbSNP Id: rs1485799371

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99152019dup , CM000671.2:g.99152019dup GRCh38
NC_000009.11:g.101914301dup , CM000671.1:g.101914301dup GRCh37
NC_000009.10:g.100954122dup NCBI36
NG_007461.1:g.51890dup

Transcript Alleles

HGVS Amino-acid change
ENST00000547314.6:c.*2714dup ENSP00000449934.2:n.*2714dup
ENST00000552573.7:c.*2714dup ENSP00000447182.3:n.*2714dup
ENST00000374994.9:c.*2714dup MANE Select ENSP00000364133.4:n.*2714dup
ENST00000374990.6:c.*2714dup ENSP00000364129.2:n.*2714dup
ENST00000374994.8:c.*2714dup ENSP00000364133.4:n.*2714dup
ENST00000552516.5:c.*2714dup ENSP00000447297.1:n.*2714dup
NM_001130916.1:c.*2714dup NP_001124388.1:n.*2714dup
NM_001130916.2:c.*2714dup NP_001124388.1:n.*2714dup
NM_001306210.1:c.*2714dup NP_001293139.1:n.*2714dup
NM_004612.2:c.*2714dup NP_004603.1:n.*2714dup
NM_004612.3:c.*2714dup NP_004603.1:n.*2714dup
XM_011518948.1:c.*2714dup XP_011517250.1:n.*2714dup
XM_011518949.1:c.*2714dup XP_011517251.1:n.*2714dup
XM_011518950.1:c.*2714dup XP_011517252.1:n.*2714dup
NM_004612.4:c.*2714dup MANE Select NP_004603.1:n.*2714dup
NM_001130916.3:c.*2714dup NP_001124388.1:n.*2714dup
NM_001306210.2:c.*2714dup NP_001293139.1:n.*2714dup