Canonical Allele Identifier: CA1867274440

Gene: TGFBR1

Linked Data

• dbSNP Id: rs1828035296

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99153792_99153794del , CM000671.2:g.99153792_99153794del	GRCh38
NC_000009.11:g.101916074_101916076del , CM000671.1:g.101916074_101916076del	GRCh37
NC_000009.10:g.100955895_100955897del	NCBI36
NG_007461.1:g.53663_53665del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.*4487_*4489del	ENSP00000449934.2:n.*4487_*4489del
ENST00000552573.7:c.*4487_*4489del	ENSP00000447182.3:n.*4487_*4489del
ENST00000374994.9:c.*4487_*4489del MANE Select	ENSP00000364133.4:n.*4487_*4489del
ENST00000374994.8:c.*4487_*4489del	ENSP00000364133.4:n.*4487_*4489del
NM_001130916.1:c.*4487_*4489del	NP_001124388.1:n.*4487_*4489del
NM_001130916.2:c.*4487_*4489del	NP_001124388.1:n.*4487_*4489del
NM_001306210.1:c.*4487_*4489del	NP_001293139.1:n.*4487_*4489del
NM_004612.2:c.*4487_*4489del	NP_004603.1:n.*4487_*4489del
NM_004612.3:c.*4487_*4489del	NP_004603.1:n.*4487_*4489del
NM_004612.4:c.*4487_*4489del MANE Select	NP_004603.1:n.*4487_*4489del
NM_001130916.3:c.*4487_*4489del	NP_001124388.1:n.*4487_*4489del
NM_001306210.2:c.*4487_*4489del	NP_001293139.1:n.*4487_*4489del