Canonical Allele Identifier: CA2585296546

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342390-C-CATT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342390_41342391insATT , CM000681.2:g.41342390_41342391insATT	GRCh38
NC_000019.9:g.41848295_41848296insATT , CM000681.1:g.41848295_41848296insATT	GRCh37
NC_000019.8:g.46540135_46540136insATT	NCBI36
NG_013364.1:g.16536_16537insAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-144_635-143insAAT MANE Select	ENSP00000221930.4:n.635-144_635-143insAAT
ENST00000600196.2:c.635-144_635-143insAAT	ENSP00000504008.1:n.635-144_635-143insAAT
ENST00000677934.1:c.634+2356_634+2357insAAT	ENSP00000504769.1:n.634+2356_634+2357insAAT
ENST00000221930.5:c.635-144_635-143insAAT	ENSP00000221930.4:n.635-144_635-143insAAT
ENST00000597453.1:n.166-144_166-143insAAT
ENST00000600196.1:n.95-144_95-143insAAT
NM_000660.5:c.635-144_635-143insAAT	NP_000651.3:n.635-144_635-143insAAT
XM_011527242.1:c.635-144_635-143insAAT	XP_011525544.1:n.635-144_635-143insAAT
NM_000660.6:c.635-144_635-143insAAT	NP_000651.3:n.635-144_635-143insAAT
XM_011527242.2:c.635-144_635-143insAAT	XP_011525544.1:n.635-144_635-143insAAT
NM_000660.7:c.635-144_635-143insAAT MANE Select	NP_000651.3:n.635-144_635-143insAAT