Canonical Allele Identifier: CA2814427076

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342376_41342377insCA , CM000681.2:g.41342376_41342377insCA	GRCh38
NC_000019.9:g.41848281_41848282insCA , CM000681.1:g.41848281_41848282insCA	GRCh37
NC_000019.8:g.46540121_46540122insCA	NCBI36
NG_013364.1:g.16550_16551insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-130_635-129insTG MANE Select	ENSP00000221930.4:n.635-130_635-129insTG
ENST00000600196.2:c.635-130_635-129insTG	ENSP00000504008.1:n.635-130_635-129insTG
ENST00000677934.1:c.634+2370_634+2371insTG	ENSP00000504769.1:n.634+2370_634+2371insTG
ENST00000221930.5:c.635-130_635-129insTG	ENSP00000221930.4:n.635-130_635-129insTG
ENST00000597453.1:n.166-130_166-129insTG
ENST00000600196.1:n.95-130_95-129insTG
NM_000660.5:c.635-130_635-129insTG	NP_000651.3:n.635-130_635-129insTG
XM_011527242.1:c.635-130_635-129insTG	XP_011525544.1:n.635-130_635-129insTG
NM_000660.6:c.635-130_635-129insTG	NP_000651.3:n.635-130_635-129insTG
XM_011527242.2:c.635-130_635-129insTG	XP_011525544.1:n.635-130_635-129insTG
NM_000660.7:c.635-130_635-129insTG MANE Select	NP_000651.3:n.635-130_635-129insTG