Canonical Allele Identifier: CA2814427092

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342388_41342389insGCGA , CM000681.2:g.41342388_41342389insGCGA	GRCh38
NC_000019.9:g.41848293_41848294insGCGA , CM000681.1:g.41848293_41848294insGCGA	GRCh37
NC_000019.8:g.46540133_46540134insGCGA	NCBI36
NG_013364.1:g.16538_16539insTCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-142_635-141insTCGC MANE Select	ENSP00000221930.4:n.635-142_635-141insTCGC
ENST00000600196.2:c.635-142_635-141insTCGC	ENSP00000504008.1:n.635-142_635-141insTCGC
ENST00000677934.1:c.634+2358_634+2359insTCGC	ENSP00000504769.1:n.634+2358_634+2359insTCGC
ENST00000221930.5:c.635-142_635-141insTCGC	ENSP00000221930.4:n.635-142_635-141insTCGC
ENST00000597453.1:n.166-142_166-141insTCGC
ENST00000600196.1:n.95-142_95-141insTCGC
NM_000660.5:c.635-142_635-141insTCGC	NP_000651.3:n.635-142_635-141insTCGC
XM_011527242.1:c.635-142_635-141insTCGC	XP_011525544.1:n.635-142_635-141insTCGC
NM_000660.6:c.635-142_635-141insTCGC	NP_000651.3:n.635-142_635-141insTCGC
XM_011527242.2:c.635-142_635-141insTCGC	XP_011525544.1:n.635-142_635-141insTCGC
NM_000660.7:c.635-142_635-141insTCGC MANE Select	NP_000651.3:n.635-142_635-141insTCGC