Canonical Allele Identifier: CA2336421222

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342388_41342394delinsCTCTTTT , CM000681.2:g.41342388_41342394delinsCTCTTTT	GRCh38
NC_000019.9:g.41848293_41848299delinsCTCTTTT , CM000681.1:g.41848293_41848299delinsCTCTTTT	GRCh37
NC_000019.8:g.46540133_46540139delinsCTCTTTT	NCBI36
NG_013364.1:g.16533_16539delinsAAAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-147_635-141delinsAAAAGAG MANE Select	ENSP00000221930.4:n.635-147_635-141delinsAAAAGAG
ENST00000600196.2:c.635-147_635-141delinsAAAAGAG	ENSP00000504008.1:n.635-147_635-141delinsAAAAGAG
ENST00000677934.1:c.634+2353_634+2359delinsAAAAGAG	ENSP00000504769.1:n.634+2353_634+2359delinsAAAAGAG
ENST00000221930.5:c.635-147_635-141delinsAAAAGAG	ENSP00000221930.4:n.635-147_635-141delinsAAAAGAG
ENST00000597453.1:n.166-147_166-141delinsAAAAGAG
ENST00000600196.1:n.95-147_95-141delinsAAAAGAG
NM_000660.5:c.635-147_635-141delinsAAAAGAG	NP_000651.3:n.635-147_635-141delinsAAAAGAG
XM_011527242.1:c.635-147_635-141delinsAAAAGAG	XP_011525544.1:n.635-147_635-141delinsAAAAGAG
NM_000660.6:c.635-147_635-141delinsAAAAGAG	NP_000651.3:n.635-147_635-141delinsAAAAGAG
XM_011527242.2:c.635-147_635-141delinsAAAAGAG	XP_011525544.1:n.635-147_635-141delinsAAAAGAG
NM_000660.7:c.635-147_635-141delinsAAAAGAG MANE Select	NP_000651.3:n.635-147_635-141delinsAAAAGAG