Canonical Allele Identifier: CA2585296505

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342385-T-TCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342386_41342387insAC , CM000681.2:g.41342386_41342387insAC	GRCh38
NC_000019.9:g.41848291_41848292insAC , CM000681.1:g.41848291_41848292insAC	GRCh37
NC_000019.8:g.46540131_46540132insAC	NCBI36
NG_013364.1:g.16541_16542insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-139_635-138insTG MANE Select	ENSP00000221930.4:n.635-139_635-138insTG
ENST00000600196.2:c.635-139_635-138insTG	ENSP00000504008.1:n.635-139_635-138insTG
ENST00000677934.1:c.634+2361_634+2362insTG	ENSP00000504769.1:n.634+2361_634+2362insTG
ENST00000221930.5:c.635-139_635-138insTG	ENSP00000221930.4:n.635-139_635-138insTG
ENST00000597453.1:n.166-139_166-138insTG
ENST00000600196.1:n.95-139_95-138insTG
NM_000660.5:c.635-139_635-138insTG	NP_000651.3:n.635-139_635-138insTG
XM_011527242.1:c.635-139_635-138insTG	XP_011525544.1:n.635-139_635-138insTG
NM_000660.6:c.635-139_635-138insTG	NP_000651.3:n.635-139_635-138insTG
XM_011527242.2:c.635-139_635-138insTG	XP_011525544.1:n.635-139_635-138insTG
NM_000660.7:c.635-139_635-138insTG MANE Select	NP_000651.3:n.635-139_635-138insTG