Canonical Allele Identifier: CA2585296538

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342390-CTTTTTTTTTTTTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342400_41342413del , CM000681.2:g.41342400_41342413del	GRCh38
NC_000019.9:g.41848305_41848318del , CM000681.1:g.41848305_41848318del	GRCh37
NC_000019.8:g.46540145_46540158del	NCBI36
NG_013364.1:g.16523_16536del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-157_635-144del MANE Select	ENSP00000221930.4:n.635-157_635-144del
ENST00000600196.2:c.635-157_635-144del	ENSP00000504008.1:n.635-157_635-144del
ENST00000677934.1:c.634+2343_634+2356del	ENSP00000504769.1:n.634+2343_634+2356del
ENST00000221930.5:c.635-157_635-144del	ENSP00000221930.4:n.635-157_635-144del
ENST00000597453.1:n.166-157_166-144del
ENST00000600196.1:n.95-157_95-144del
NM_000660.5:c.635-157_635-144del	NP_000651.3:n.635-157_635-144del
XM_011527242.1:c.635-157_635-144del	XP_011525544.1:n.635-157_635-144del
NM_000660.6:c.635-157_635-144del	NP_000651.3:n.635-157_635-144del
XM_011527242.2:c.635-157_635-144del	XP_011525544.1:n.635-157_635-144del
NM_000660.7:c.635-157_635-144del MANE Select	NP_000651.3:n.635-157_635-144del