Canonical Allele Identifier: CA2336421206

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342368_41342369delinsTG , CM000681.2:g.41342368_41342369delinsTG	GRCh38
NC_000019.9:g.41848273_41848274delinsTG , CM000681.1:g.41848273_41848274delinsTG	GRCh37
NC_000019.8:g.46540113_46540114delinsTG	NCBI36
NG_013364.1:g.16558_16559delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-122_635-121delinsCA MANE Select	ENSP00000221930.4:n.635-122_635-121delinsCA
ENST00000600196.2:c.635-122_635-121delinsCA	ENSP00000504008.1:n.635-122_635-121delinsCA
ENST00000677934.1:c.634+2378_634+2379delinsCA	ENSP00000504769.1:n.634+2378_634+2379delinsCA
ENST00000221930.5:c.635-122_635-121delinsCA	ENSP00000221930.4:n.635-122_635-121delinsCA
ENST00000597453.1:n.166-122_166-121delinsCA
ENST00000600196.1:n.95-122_95-121delinsCA
NM_000660.5:c.635-122_635-121delinsCA	NP_000651.3:n.635-122_635-121delinsCA
XM_011527242.1:c.635-122_635-121delinsCA	XP_011525544.1:n.635-122_635-121delinsCA
NM_000660.6:c.635-122_635-121delinsCA	NP_000651.3:n.635-122_635-121delinsCA
XM_011527242.2:c.635-122_635-121delinsCA	XP_011525544.1:n.635-122_635-121delinsCA
NM_000660.7:c.635-122_635-121delinsCA MANE Select	NP_000651.3:n.635-122_635-121delinsCA