Canonical Allele Identifier: CA2531476600

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342384_41342385insCC , CM000681.2:g.41342384_41342385insCC	GRCh38
NC_000019.9:g.41848289_41848290insCC , CM000681.1:g.41848289_41848290insCC	GRCh37
NC_000019.8:g.46540129_46540130insCC	NCBI36
NG_013364.1:g.16543_16544insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-137_635-136insGG MANE Select	ENSP00000221930.4:n.635-137_635-136insGG
ENST00000600196.2:c.635-137_635-136insGG	ENSP00000504008.1:n.635-137_635-136insGG
ENST00000677934.1:c.634+2363_634+2364insGG	ENSP00000504769.1:n.634+2363_634+2364insGG
ENST00000221930.5:c.635-137_635-136insGG	ENSP00000221930.4:n.635-137_635-136insGG
ENST00000597453.1:n.166-137_166-136insGG
ENST00000600196.1:n.95-137_95-136insGG
NM_000660.5:c.635-137_635-136insGG	NP_000651.3:n.635-137_635-136insGG
XM_011527242.1:c.635-137_635-136insGG	XP_011525544.1:n.635-137_635-136insGG
NM_000660.6:c.635-137_635-136insGG	NP_000651.3:n.635-137_635-136insGG
XM_011527242.2:c.635-137_635-136insGG	XP_011525544.1:n.635-137_635-136insGG
NM_000660.7:c.635-137_635-136insGG MANE Select	NP_000651.3:n.635-137_635-136insGG