Canonical Allele Identifier: CA2585296533

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342389-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342389_41342390insAA , CM000681.2:g.41342389_41342390insAA	GRCh38
NC_000019.9:g.41848294_41848295insAA , CM000681.1:g.41848294_41848295insAA	GRCh37
NC_000019.8:g.46540134_46540135insAA	NCBI36
NG_013364.1:g.16537_16538insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-143_635-142insTT MANE Select	ENSP00000221930.4:n.635-143_635-142insTT
ENST00000600196.2:c.635-143_635-142insTT	ENSP00000504008.1:n.635-143_635-142insTT
ENST00000677934.1:c.634+2357_634+2358insTT	ENSP00000504769.1:n.634+2357_634+2358insTT
ENST00000221930.5:c.635-143_635-142insTT	ENSP00000221930.4:n.635-143_635-142insTT
ENST00000597453.1:n.166-143_166-142insTT
ENST00000600196.1:n.95-143_95-142insTT
NM_000660.5:c.635-143_635-142insTT	NP_000651.3:n.635-143_635-142insTT
XM_011527242.1:c.635-143_635-142insTT	XP_011525544.1:n.635-143_635-142insTT
NM_000660.6:c.635-143_635-142insTT	NP_000651.3:n.635-143_635-142insTT
XM_011527242.2:c.635-143_635-142insTT	XP_011525544.1:n.635-143_635-142insTT
NM_000660.7:c.635-143_635-142insTT MANE Select	NP_000651.3:n.635-143_635-142insTT