Canonical Allele Identifier: CA2585296500

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342384-C-CCA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342384_41342385insCA , CM000681.2:g.41342384_41342385insCA	GRCh38
NC_000019.9:g.41848289_41848290insCA , CM000681.1:g.41848289_41848290insCA	GRCh37
NC_000019.8:g.46540129_46540130insCA	NCBI36
NG_013364.1:g.16542_16543insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-138_635-137insTG MANE Select	ENSP00000221930.4:n.635-138_635-137insTG
ENST00000600196.2:c.635-138_635-137insTG	ENSP00000504008.1:n.635-138_635-137insTG
ENST00000677934.1:c.634+2362_634+2363insTG	ENSP00000504769.1:n.634+2362_634+2363insTG
ENST00000221930.5:c.635-138_635-137insTG	ENSP00000221930.4:n.635-138_635-137insTG
ENST00000597453.1:n.166-138_166-137insTG
ENST00000600196.1:n.95-138_95-137insTG
NM_000660.5:c.635-138_635-137insTG	NP_000651.3:n.635-138_635-137insTG
XM_011527242.1:c.635-138_635-137insTG	XP_011525544.1:n.635-138_635-137insTG
NM_000660.6:c.635-138_635-137insTG	NP_000651.3:n.635-138_635-137insTG
XM_011527242.2:c.635-138_635-137insTG	XP_011525544.1:n.635-138_635-137insTG
NM_000660.7:c.635-138_635-137insTG MANE Select	NP_000651.3:n.635-138_635-137insTG