Canonical Allele Identifier: CA2814427078

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342381_41342382insCCCGCG , CM000681.2:g.41342381_41342382insCCCGCG	GRCh38
NC_000019.9:g.41848286_41848287insCCCGCG , CM000681.1:g.41848286_41848287insCCCGCG	GRCh37
NC_000019.8:g.46540126_46540127insCCCGCG	NCBI36
NG_013364.1:g.16545_16546insCGCGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-135_635-134insCGCGGG MANE Select	ENSP00000221930.4:n.635-135_635-134insCGCGGG
ENST00000600196.2:c.635-135_635-134insCGCGGG	ENSP00000504008.1:n.635-135_635-134insCGCGGG
ENST00000677934.1:c.634+2365_634+2366insCGCGGG	ENSP00000504769.1:n.634+2365_634+2366insCGCGGG
ENST00000221930.5:c.635-135_635-134insCGCGGG	ENSP00000221930.4:n.635-135_635-134insCGCGGG
ENST00000597453.1:n.166-135_166-134insCGCGGG
ENST00000600196.1:n.95-135_95-134insCGCGGG
NM_000660.5:c.635-135_635-134insCGCGGG	NP_000651.3:n.635-135_635-134insCGCGGG
XM_011527242.1:c.635-135_635-134insCGCGGG	XP_011525544.1:n.635-135_635-134insCGCGGG
NM_000660.6:c.635-135_635-134insCGCGGG	NP_000651.3:n.635-135_635-134insCGCGGG
XM_011527242.2:c.635-135_635-134insCGCGGG	XP_011525544.1:n.635-135_635-134insCGCGGG
NM_000660.7:c.635-135_635-134insCGCGGG MANE Select	NP_000651.3:n.635-135_635-134insCGCGGG