Canonical Allele Identifier: CA1867274439

Gene: TGFBR1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99153788_99153791delinsATAT , CM000671.2:g.99153788_99153791delinsATAT	GRCh38
NC_000009.11:g.101916070_101916073delinsATAT , CM000671.1:g.101916070_101916073delinsATAT	GRCh37
NC_000009.10:g.100955891_100955894delinsATAT	NCBI36
NG_007461.1:g.53659_53662delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.*4483_*4486delinsATAT	ENSP00000449934.2:n.*4483_*4486delinsATAT
ENST00000552573.7:c.*4483_*4486delinsATAT	ENSP00000447182.3:n.*4483_*4486delinsATAT
ENST00000374994.9:c.*4483_*4486delinsATAT MANE Select	ENSP00000364133.4:n.*4483_*4486delinsATAT
ENST00000374994.8:c.*4483_*4486delinsATAT	ENSP00000364133.4:n.*4483_*4486delinsATAT
NM_001130916.1:c.*4483_*4486delinsATAT	NP_001124388.1:n.*4483_*4486delinsATAT
NM_001130916.2:c.*4483_*4486delinsATAT	NP_001124388.1:n.*4483_*4486delinsATAT
NM_001306210.1:c.*4483_*4486delinsATAT	NP_001293139.1:n.*4483_*4486delinsATAT
NM_004612.2:c.*4483_*4486delinsATAT	NP_004603.1:n.*4483_*4486delinsATAT
NM_004612.3:c.*4483_*4486delinsATAT	NP_004603.1:n.*4483_*4486delinsATAT
NM_004612.4:c.*4483_*4486delinsATAT MANE Select	NP_004603.1:n.*4483_*4486delinsATAT
NM_001130916.3:c.*4483_*4486delinsATAT	NP_001124388.1:n.*4483_*4486delinsATAT
NM_001306210.2:c.*4483_*4486delinsATAT	NP_001293139.1:n.*4483_*4486delinsATAT