Canonical Allele Identifier: CA2814427073
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342366_41342368del , CM000681.2:g.41342366_41342368del GRCh38
NC_000019.9:g.41848271_41848273del , CM000681.1:g.41848271_41848273del GRCh37
NC_000019.8:g.46540111_46540113del NCBI36
NG_013364.1:g.16559_16561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-121_635-119del MANE Select ENSP00000221930.4:n.635-121_635-119del
ENST00000600196.2:c.635-121_635-119del ENSP00000504008.1:n.635-121_635-119del
ENST00000677934.1:c.634+2379_634+2381del ENSP00000504769.1:n.634+2379_634+2381del
ENST00000221930.5:c.635-121_635-119del ENSP00000221930.4:n.635-121_635-119del
ENST00000597453.1:n.166-121_166-119del
ENST00000600196.1:n.95-121_95-119del
NM_000660.5:c.635-121_635-119del NP_000651.3:n.635-121_635-119del
XM_011527242.1:c.635-121_635-119del XP_011525544.1:n.635-121_635-119del
NM_000660.6:c.635-121_635-119del NP_000651.3:n.635-121_635-119del
XM_011527242.2:c.635-121_635-119del XP_011525544.1:n.635-121_635-119del
NM_000660.7:c.635-121_635-119del MANE Select NP_000651.3:n.635-121_635-119del