Canonical Allele Identifier: CA2336421160

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342277_41342279delinsTGA , CM000681.2:g.41342277_41342279delinsTGA	GRCh38
NC_000019.9:g.41848182_41848184delinsTGA , CM000681.1:g.41848182_41848184delinsTGA	GRCh37
NC_000019.8:g.46540022_46540024delinsTGA	NCBI36
NG_013364.1:g.16648_16650delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-32_635-30delinsTCA MANE Select	ENSP00000221930.4:n.635-32_635-30delinsTCA
ENST00000600196.2:c.635-32_635-30delinsTCA	ENSP00000504008.1:n.635-32_635-30delinsTCA
ENST00000677934.1:c.634+2468_634+2470delinsTCA	ENSP00000504769.1:n.634+2468_634+2470delinsTCA
ENST00000221930.5:c.635-32_635-30delinsTCA	ENSP00000221930.4:n.635-32_635-30delinsTCA
ENST00000597453.1:n.166-32_166-30delinsTCA
ENST00000600196.1:n.95-32_95-30delinsTCA
NM_000660.5:c.635-32_635-30delinsTCA	NP_000651.3:n.635-32_635-30delinsTCA
XM_011527242.1:c.635-32_635-30delinsTCA	XP_011525544.1:n.635-32_635-30delinsTCA
NM_000660.6:c.635-32_635-30delinsTCA	NP_000651.3:n.635-32_635-30delinsTCA
XM_011527242.2:c.635-32_635-30delinsTCA	XP_011525544.1:n.635-32_635-30delinsTCA
NM_000660.7:c.635-32_635-30delinsTCA MANE Select	NP_000651.3:n.635-32_635-30delinsTCA