Canonical Allele Identifier: CA2585296532

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342389-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342389_41342390insA , CM000681.2:g.41342389_41342390insA	GRCh38
NC_000019.9:g.41848294_41848295insA , CM000681.1:g.41848294_41848295insA	GRCh37
NC_000019.8:g.46540134_46540135insA	NCBI36
NG_013364.1:g.16537_16538insT

Transcript Alleles

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