Canonical Allele Identifier: CA2585296528

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342388-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342388_41342389insAA , CM000681.2:g.41342388_41342389insAA	GRCh38
NC_000019.9:g.41848293_41848294insAA , CM000681.1:g.41848293_41848294insAA	GRCh37
NC_000019.8:g.46540133_46540134insAA	NCBI36
NG_013364.1:g.16538_16539insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-142_635-141insTT MANE Select	ENSP00000221930.4:n.635-142_635-141insTT
ENST00000600196.2:c.635-142_635-141insTT	ENSP00000504008.1:n.635-142_635-141insTT
ENST00000677934.1:c.634+2358_634+2359insTT	ENSP00000504769.1:n.634+2358_634+2359insTT
ENST00000221930.5:c.635-142_635-141insTT	ENSP00000221930.4:n.635-142_635-141insTT
ENST00000597453.1:n.166-142_166-141insTT
ENST00000600196.1:n.95-142_95-141insTT
NM_000660.5:c.635-142_635-141insTT	NP_000651.3:n.635-142_635-141insTT
XM_011527242.1:c.635-142_635-141insTT	XP_011525544.1:n.635-142_635-141insTT
NM_000660.6:c.635-142_635-141insTT	NP_000651.3:n.635-142_635-141insTT
XM_011527242.2:c.635-142_635-141insTT	XP_011525544.1:n.635-142_635-141insTT
NM_000660.7:c.635-142_635-141insTT MANE Select	NP_000651.3:n.635-142_635-141insTT