Canonical Allele Identifier: CA869146352

Gene: TGFBR1

Linked Data

• dbSNP Id: rs1174443028
• MyVariant Identifiers: chr9:g.101915914A>C (hg19) ; chr9:g.99153632A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99153632A>C , CM000671.2:g.99153632A>C	GRCh38
NC_000009.11:g.101915914A>C , CM000671.1:g.101915914A>C	GRCh37
NC_000009.10:g.100955735A>C	NCBI36
NG_007461.1:g.53503A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547314.6:c.*4327A>C	ENSP00000449934.2:n.*4327A>C
ENST00000552573.7:c.*4327A>C	ENSP00000447182.3:n.*4327A>C
ENST00000374994.9:c.*4327A>C MANE Select	ENSP00000364133.4:n.*4327A>C
ENST00000374990.6:c.*4327A>C	ENSP00000364129.2:n.*4327A>C
ENST00000374994.8:c.*4327A>C	ENSP00000364133.4:n.*4327A>C
ENST00000552516.5:c.*4327A>C	ENSP00000447297.1:n.*4327A>C
NM_001130916.1:c.*4327A>C	NP_001124388.1:n.*4327A>C
NM_001130916.2:c.*4327A>C	NP_001124388.1:n.*4327A>C
NM_001306210.1:c.*4327A>C	NP_001293139.1:n.*4327A>C
NM_004612.2:c.*4327A>C	NP_004603.1:n.*4327A>C
NM_004612.3:c.*4327A>C	NP_004603.1:n.*4327A>C
XM_011518948.1:c.*4327A>C	XP_011517250.1:n.*4327A>C
XM_011518949.1:c.*4327A>C	XP_011517251.1:n.*4327A>C
XM_011518950.1:c.*4327A>C	XP_011517252.1:n.*4327A>C
NM_004612.4:c.*4327A>C MANE Select	NP_004603.1:n.*4327A>C
NM_001130916.3:c.*4327A>C	NP_001124388.1:n.*4327A>C
NM_001306210.2:c.*4327A>C	NP_001293139.1:n.*4327A>C