Canonical Allele Identifier: CA2585296244

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41332410-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332411_41332412insGG , CM000681.2:g.41332411_41332412insGG	GRCh38
NC_000019.9:g.41838316_41838317insGG , CM000681.1:g.41838316_41838317insGG	GRCh37
NC_000019.8:g.46530156_46530157insGG	NCBI36
NG_013364.1:g.26516_26517insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-130_861-129insCC MANE Select	ENSP00000221930.4:n.861-130_861-129insCC
ENST00000600196.2:c.713-130_713-129insCC	ENSP00000504008.1:n.713-130_713-129insCC
ENST00000677934.1:c.635-130_635-129insCC	ENSP00000504769.1:n.635-130_635-129insCC
ENST00000221930.5:c.861-130_861-129insCC	ENSP00000221930.4:n.861-130_861-129insCC
ENST00000598758.5:c.149-130_149-129insCC
ENST00000600196.1:n.173-130_173-129insCC
NM_000660.5:c.861-130_861-129insCC	NP_000651.3:n.861-130_861-129insCC
XM_011527242.1:c.864-130_864-129insCC	XP_011525544.1:n.864-130_864-129insCC
NM_000660.6:c.861-130_861-129insCC	NP_000651.3:n.861-130_861-129insCC
XM_011527242.2:c.864-130_864-129insCC	XP_011525544.1:n.864-130_864-129insCC
NM_000660.7:c.861-130_861-129insCC MANE Select	NP_000651.3:n.861-130_861-129insCC