Canonical Allele Identifier: CA2585296551

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342391-T-TAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342391_41342392insAAA , CM000681.2:g.41342391_41342392insAAA	GRCh38
NC_000019.9:g.41848296_41848297insAAA , CM000681.1:g.41848296_41848297insAAA	GRCh37
NC_000019.8:g.46540136_46540137insAAA	NCBI36
NG_013364.1:g.16535_16536insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-145_635-144insTTT MANE Select	ENSP00000221930.4:n.635-145_635-144insTTT
ENST00000600196.2:c.635-145_635-144insTTT	ENSP00000504008.1:n.635-145_635-144insTTT
ENST00000677934.1:c.634+2355_634+2356insTTT	ENSP00000504769.1:n.634+2355_634+2356insTTT
ENST00000221930.5:c.635-145_635-144insTTT	ENSP00000221930.4:n.635-145_635-144insTTT
ENST00000597453.1:n.166-145_166-144insTTT
ENST00000600196.1:n.95-145_95-144insTTT
NM_000660.5:c.635-145_635-144insTTT	NP_000651.3:n.635-145_635-144insTTT
XM_011527242.1:c.635-145_635-144insTTT	XP_011525544.1:n.635-145_635-144insTTT
NM_000660.6:c.635-145_635-144insTTT	NP_000651.3:n.635-145_635-144insTTT
XM_011527242.2:c.635-145_635-144insTTT	XP_011525544.1:n.635-145_635-144insTTT
NM_000660.7:c.635-145_635-144insTTT MANE Select	NP_000651.3:n.635-145_635-144insTTT