Canonical Allele Identifier: CA2814427079

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342382_41342383insAGG , CM000681.2:g.41342382_41342383insAGG	GRCh38
NC_000019.9:g.41848287_41848288insAGG , CM000681.1:g.41848287_41848288insAGG	GRCh37
NC_000019.8:g.46540127_46540128insAGG	NCBI36
NG_013364.1:g.16544_16545insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-136_635-135insCCT MANE Select	ENSP00000221930.4:n.635-136_635-135insCCT
ENST00000600196.2:c.635-136_635-135insCCT	ENSP00000504008.1:n.635-136_635-135insCCT
ENST00000677934.1:c.634+2364_634+2365insCCT	ENSP00000504769.1:n.634+2364_634+2365insCCT
ENST00000221930.5:c.635-136_635-135insCCT	ENSP00000221930.4:n.635-136_635-135insCCT
ENST00000597453.1:n.166-136_166-135insCCT
ENST00000600196.1:n.95-136_95-135insCCT
NM_000660.5:c.635-136_635-135insCCT	NP_000651.3:n.635-136_635-135insCCT
XM_011527242.1:c.635-136_635-135insCCT	XP_011525544.1:n.635-136_635-135insCCT
NM_000660.6:c.635-136_635-135insCCT	NP_000651.3:n.635-136_635-135insCCT
XM_011527242.2:c.635-136_635-135insCCT	XP_011525544.1:n.635-136_635-135insCCT
NM_000660.7:c.635-136_635-135insCCT MANE Select	NP_000651.3:n.635-136_635-135insCCT