Canonical Allele Identifier: CA2582167004
Gene: TGFB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41342392_41342393insAATAAA , CM000681.2:g.41342392_41342393insAATAAA GRCh38
NC_000019.9:g.41848297_41848298insAATAAA , CM000681.1:g.41848297_41848298insAATAAA GRCh37
NC_000019.8:g.46540137_46540138insAATAAA NCBI36
NG_013364.1:g.16534_16535insTTTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.635-146_635-145insTTTATT MANE Select ENSP00000221930.4:n.635-146_635-145insTTTATT
ENST00000600196.2:c.635-146_635-145insTTTATT ENSP00000504008.1:n.635-146_635-145insTTTATT
ENST00000677934.1:c.634+2354_634+2355insTTTATT ENSP00000504769.1:n.634+2354_634+2355insTTTATT
ENST00000221930.5:c.635-146_635-145insTTTATT ENSP00000221930.4:n.635-146_635-145insTTTATT
ENST00000597453.1:n.166-146_166-145insTTTATT
ENST00000600196.1:n.95-146_95-145insTTTATT
NM_000660.5:c.635-146_635-145insTTTATT NP_000651.3:n.635-146_635-145insTTTATT
XM_011527242.1:c.635-146_635-145insTTTATT XP_011525544.1:n.635-146_635-145insTTTATT
NM_000660.6:c.635-146_635-145insTTTATT NP_000651.3:n.635-146_635-145insTTTATT
XM_011527242.2:c.635-146_635-145insTTTATT XP_011525544.1:n.635-146_635-145insTTTATT
NM_000660.7:c.635-146_635-145insTTTATT MANE Select NP_000651.3:n.635-146_635-145insTTTATT