Canonical Allele Identifier: CA2814427066

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342356_41342357insA , CM000681.2:g.41342356_41342357insA	GRCh38
NC_000019.9:g.41848261_41848262insA , CM000681.1:g.41848261_41848262insA	GRCh37
NC_000019.8:g.46540101_46540102insA	NCBI36
NG_013364.1:g.16570_16571insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-110_635-109insT MANE Select	ENSP00000221930.4:n.635-110_635-109insT
ENST00000600196.2:c.635-110_635-109insT	ENSP00000504008.1:n.635-110_635-109insT
ENST00000677934.1:c.634+2390_634+2391insT	ENSP00000504769.1:n.634+2390_634+2391insT
ENST00000221930.5:c.635-110_635-109insT	ENSP00000221930.4:n.635-110_635-109insT
ENST00000597453.1:n.166-110_166-109insT
ENST00000600196.1:n.95-110_95-109insT
NM_000660.5:c.635-110_635-109insT	NP_000651.3:n.635-110_635-109insT
XM_011527242.1:c.635-110_635-109insT	XP_011525544.1:n.635-110_635-109insT
NM_000660.6:c.635-110_635-109insT	NP_000651.3:n.635-110_635-109insT
XM_011527242.2:c.635-110_635-109insT	XP_011525544.1:n.635-110_635-109insT
NM_000660.7:c.635-110_635-109insT MANE Select	NP_000651.3:n.635-110_635-109insT