Canonical Allele Identifier: CA2585296522

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342387-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342387_41342388insAA , CM000681.2:g.41342387_41342388insAA	GRCh38
NC_000019.9:g.41848292_41848293insAA , CM000681.1:g.41848292_41848293insAA	GRCh37
NC_000019.8:g.46540132_46540133insAA	NCBI36
NG_013364.1:g.16539_16540insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-141_635-140insTT MANE Select	ENSP00000221930.4:n.635-141_635-140insTT
ENST00000600196.2:c.635-141_635-140insTT	ENSP00000504008.1:n.635-141_635-140insTT
ENST00000677934.1:c.634+2359_634+2360insTT	ENSP00000504769.1:n.634+2359_634+2360insTT
ENST00000221930.5:c.635-141_635-140insTT	ENSP00000221930.4:n.635-141_635-140insTT
ENST00000597453.1:n.166-141_166-140insTT
ENST00000600196.1:n.95-141_95-140insTT
NM_000660.5:c.635-141_635-140insTT	NP_000651.3:n.635-141_635-140insTT
XM_011527242.1:c.635-141_635-140insTT	XP_011525544.1:n.635-141_635-140insTT
NM_000660.6:c.635-141_635-140insTT	NP_000651.3:n.635-141_635-140insTT
XM_011527242.2:c.635-141_635-140insTT	XP_011525544.1:n.635-141_635-140insTT
NM_000660.7:c.635-141_635-140insTT MANE Select	NP_000651.3:n.635-141_635-140insTT