Canonical Allele Identifier: CA995955879
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342423_41342424insTTTTTTTTTTTTT , CM000681.2:g.41342423_41342424insTTTTTTTTTTTTT GRCh38
NC_000019.9:g.41848328_41848329insTTTTTTTTTTTTT , CM000681.1:g.41848328_41848329insTTTTTTTTTTTTT GRCh37
NC_000019.8:g.46540168_46540169insTTTTTTTTTTTTT NCBI36
NG_013364.1:g.16504_16505insAAAAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-176_635-175insAAAAAAAAAAAAA MANE Select ENSP00000221930.4:n.635-176_635-175insAAAAAAAAAAAAA
ENST00000600196.2:c.635-176_635-175insAAAAAAAAAAAAA ENSP00000504008.1:n.635-176_635-175insAAAAAAAAAAAAA
ENST00000677934.1:c.634+2324_634+2325insAAAAAAAAAAAAA ENSP00000504769.1:n.634+2324_634+2325insAAAAAAAAAAAAA
ENST00000221930.5:c.635-176_635-175insAAAAAAAAAAAAA ENSP00000221930.4:n.635-176_635-175insAAAAAAAAAAAAA
ENST00000597453.1:n.166-176_166-175insAAAAAAAAAAAAA
ENST00000600196.1:n.95-176_95-175insAAAAAAAAAAAAA
NM_000660.5:c.635-176_635-175insAAAAAAAAAAAAA NP_000651.3:n.635-176_635-175insAAAAAAAAAAAAA
XM_011527242.1:c.635-176_635-175insAAAAAAAAAAAAA XP_011525544.1:n.635-176_635-175insAAAAAAAAAAAAA
NM_000660.6:c.635-176_635-175insAAAAAAAAAAAAA NP_000651.3:n.635-176_635-175insAAAAAAAAAAAAA
XM_011527242.2:c.635-176_635-175insAAAAAAAAAAAAA XP_011525544.1:n.635-176_635-175insAAAAAAAAAAAAA
NM_000660.7:c.635-176_635-175insAAAAAAAAAAAAA MANE Select NP_000651.3:n.635-176_635-175insAAAAAAAAAAAAA