Canonical Allele Identifier: CA1867274999
Gene: TGFBR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.99154090A= , CM000671.2:g.99154090A= GRCh38
NC_000009.11:g.101916372A= , CM000671.1:g.101916372A= GRCh37
NC_000009.10:g.100956193A= NCBI36
NG_007461.1:g.53961A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000547314.6:c.*4785A= ENSP00000449934.2:n.*4785A=
ENST00000552573.7:c.*4785A= ENSP00000447182.3:n.*4785A=
ENST00000374994.9:c.*4785A= MANE Select ENSP00000364133.4:n.*4785A=
ENST00000374994.8:c.*4785A= ENSP00000364133.4:n.*4785A=
NM_001130916.1:c.*4785A= NP_001124388.1:n.*4785A=
NM_001130916.2:c.*4785A= NP_001124388.1:n.*4785A=
NM_001306210.1:c.*4785A= NP_001293139.1:n.*4785A=
NM_004612.2:c.*4785A= NP_004603.1:n.*4785A=
NM_004612.3:c.*4785A= NP_004603.1:n.*4785A=
NM_004612.4:c.*4785A= MANE Select NP_004603.1:n.*4785A=
NM_001130916.3:c.*4785A= NP_001124388.1:n.*4785A=
NM_001306210.2:c.*4785A= NP_001293139.1:n.*4785A=
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