Canonical Allele Identifier: CA2690968229

Gene: TGFBR1

Linked Data

• gnomAD v4: 9-99153960-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99153960A>G , CM000671.2:g.99153960A>G	GRCh38
NC_000009.11:g.101916242A>G , CM000671.1:g.101916242A>G	GRCh37
NC_000009.10:g.100956063A>G	NCBI36
NG_007461.1:g.53831A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.*4655A>G	ENSP00000449934.2:n.*4655A>G
ENST00000552573.7:c.*4655A>G	ENSP00000447182.3:n.*4655A>G
ENST00000374994.9:c.*4655A>G MANE Select	ENSP00000364133.4:n.*4655A>G
ENST00000374994.8:c.*4655A>G	ENSP00000364133.4:n.*4655A>G
NM_001130916.1:c.*4655A>G	NP_001124388.1:n.*4655A>G
NM_001130916.2:c.*4655A>G	NP_001124388.1:n.*4655A>G
NM_001306210.1:c.*4655A>G	NP_001293139.1:n.*4655A>G
NM_004612.2:c.*4655A>G	NP_004603.1:n.*4655A>G
NM_004612.3:c.*4655A>G	NP_004603.1:n.*4655A>G
NM_004612.4:c.*4655A>G MANE Select	NP_004603.1:n.*4655A>G
NM_001130916.3:c.*4655A>G	NP_001124388.1:n.*4655A>G
NM_001306210.2:c.*4655A>G	NP_001293139.1:n.*4655A>G