Canonical Allele Identifier: CA10634335

Gene: TGFBR1

Linked Data

• ClinVar Variation Id: 364171
• ClinVar RCV Id: RCV000297519 ; RCV000336133 ; RCV000400688
• dbSNP Id: rs886063252
• MyVariant Identifiers: chr9:g.101915154G>A (hg19) ; chr9:g.99152872G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.99152872G>A , CM000671.2:g.99152872G>A	GRCh38
NC_000009.11:g.101915154G>A , CM000671.1:g.101915154G>A	GRCh37
NC_000009.10:g.100954975G>A	NCBI36
NG_007461.1:g.52743G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000547314.6:c.*3567G>A	ENSP00000449934.2:n.*3567G>A
ENST00000552573.7:c.*3567G>A	ENSP00000447182.3:n.*3567G>A
ENST00000374994.9:c.*3567G>A MANE Select	ENSP00000364133.4:n.*3567G>A
ENST00000374990.6:c.*3567G>A	ENSP00000364129.2:n.*3567G>A
ENST00000374994.8:c.*3567G>A	ENSP00000364133.4:n.*3567G>A
ENST00000552516.5:c.*3567G>A	ENSP00000447297.1:n.*3567G>A
NM_001130916.1:c.*3567G>A	NP_001124388.1:n.*3567G>A
NM_001130916.2:c.*3567G>A	NP_001124388.1:n.*3567G>A
NM_001306210.1:c.*3567G>A	NP_001293139.1:n.*3567G>A
NM_004612.2:c.*3567G>A	NP_004603.1:n.*3567G>A
NM_004612.3:c.*3567G>A	NP_004603.1:n.*3567G>A
XM_011518948.1:c.*3567G>A	XP_011517250.1:n.*3567G>A
XM_011518949.1:c.*3567G>A	XP_011517251.1:n.*3567G>A
XM_011518950.1:c.*3567G>A	XP_011517252.1:n.*3567G>A
NM_004612.4:c.*3567G>A MANE Select	NP_004603.1:n.*3567G>A
NM_001130916.3:c.*3567G>A	NP_001124388.1:n.*3567G>A
NM_001306210.2:c.*3567G>A	NP_001293139.1:n.*3567G>A