Canonical Allele Identifier: CA2585296554

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342393-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342393_41342394insAA , CM000681.2:g.41342393_41342394insAA	GRCh38
NC_000019.9:g.41848298_41848299insAA , CM000681.1:g.41848298_41848299insAA	GRCh37
NC_000019.8:g.46540138_46540139insAA	NCBI36
NG_013364.1:g.16533_16534insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-147_635-146insTT MANE Select	ENSP00000221930.4:n.635-147_635-146insTT
ENST00000600196.2:c.635-147_635-146insTT	ENSP00000504008.1:n.635-147_635-146insTT
ENST00000677934.1:c.634+2353_634+2354insTT	ENSP00000504769.1:n.634+2353_634+2354insTT
ENST00000221930.5:c.635-147_635-146insTT	ENSP00000221930.4:n.635-147_635-146insTT
ENST00000597453.1:n.166-147_166-146insTT
ENST00000600196.1:n.95-147_95-146insTT
NM_000660.5:c.635-147_635-146insTT	NP_000651.3:n.635-147_635-146insTT
XM_011527242.1:c.635-147_635-146insTT	XP_011525544.1:n.635-147_635-146insTT
NM_000660.6:c.635-147_635-146insTT	NP_000651.3:n.635-147_635-146insTT
XM_011527242.2:c.635-147_635-146insTT	XP_011525544.1:n.635-147_635-146insTT
NM_000660.7:c.635-147_635-146insTT MANE Select	NP_000651.3:n.635-147_635-146insTT