Canonical Allele Identifier: CA2585296543

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342390-C-CAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342390_41342391insAAAA , CM000681.2:g.41342390_41342391insAAAA	GRCh38
NC_000019.9:g.41848295_41848296insAAAA , CM000681.1:g.41848295_41848296insAAAA	GRCh37
NC_000019.8:g.46540135_46540136insAAAA	NCBI36
NG_013364.1:g.16536_16537insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-144_635-143insTTTT MANE Select	ENSP00000221930.4:n.635-144_635-143insTTTT
ENST00000600196.2:c.635-144_635-143insTTTT	ENSP00000504008.1:n.635-144_635-143insTTTT
ENST00000677934.1:c.634+2356_634+2357insTTTT	ENSP00000504769.1:n.634+2356_634+2357insTTTT
ENST00000221930.5:c.635-144_635-143insTTTT	ENSP00000221930.4:n.635-144_635-143insTTTT
ENST00000597453.1:n.166-144_166-143insTTTT
ENST00000600196.1:n.95-144_95-143insTTTT
NM_000660.5:c.635-144_635-143insTTTT	NP_000651.3:n.635-144_635-143insTTTT
XM_011527242.1:c.635-144_635-143insTTTT	XP_011525544.1:n.635-144_635-143insTTTT
NM_000660.6:c.635-144_635-143insTTTT	NP_000651.3:n.635-144_635-143insTTTT
XM_011527242.2:c.635-144_635-143insTTTT	XP_011525544.1:n.635-144_635-143insTTTT
NM_000660.7:c.635-144_635-143insTTTT MANE Select	NP_000651.3:n.635-144_635-143insTTTT