Canonical Allele Identifier: CA995955794
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342414_41342422del , CM000681.2:g.41342414_41342422del GRCh38
NC_000019.9:g.41848319_41848327del , CM000681.1:g.41848319_41848327del GRCh37
NC_000019.8:g.46540159_46540167del NCBI36
NG_013364.1:g.16505_16513del

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-175_635-167del MANE Select ENSP00000221930.4:n.635-175_635-167del
ENST00000600196.2:c.635-175_635-167del ENSP00000504008.1:n.635-175_635-167del
ENST00000677934.1:c.634+2325_634+2333del ENSP00000504769.1:n.634+2325_634+2333del
ENST00000221930.5:c.635-175_635-167del ENSP00000221930.4:n.635-175_635-167del
ENST00000597453.1:n.166-175_166-167del
ENST00000600196.1:n.95-175_95-167del
NM_000660.5:c.635-175_635-167del NP_000651.3:n.635-175_635-167del
XM_011527242.1:c.635-175_635-167del XP_011525544.1:n.635-175_635-167del
NM_000660.6:c.635-175_635-167del NP_000651.3:n.635-175_635-167del
XM_011527242.2:c.635-175_635-167del XP_011525544.1:n.635-175_635-167del
NM_000660.7:c.635-175_635-167del MANE Select NP_000651.3:n.635-175_635-167del