Canonical Allele Identifier: CA2336416559

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332418_41332420delinsCTG , CM000681.2:g.41332418_41332420delinsCTG	GRCh38
NC_000019.9:g.41838323_41838325delinsCTG , CM000681.1:g.41838323_41838325delinsCTG	GRCh37
NC_000019.8:g.46530163_46530165delinsCTG	NCBI36
NG_013364.1:g.26507_26509delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-139_861-137delinsCAG MANE Select	ENSP00000221930.4:n.861-139_861-137delinsCAG
ENST00000600196.2:c.713-139_713-137delinsCAG	ENSP00000504008.1:n.713-139_713-137delinsCAG
ENST00000677934.1:c.635-139_635-137delinsCAG	ENSP00000504769.1:n.635-139_635-137delinsCAG
ENST00000221930.5:c.861-139_861-137delinsCAG	ENSP00000221930.4:n.861-139_861-137delinsCAG
ENST00000598758.5:c.149-139_149-137delinsCAG
ENST00000600196.1:n.173-139_173-137delinsCAG
NM_000660.5:c.861-139_861-137delinsCAG	NP_000651.3:n.861-139_861-137delinsCAG
XM_011527242.1:c.864-139_864-137delinsCAG	XP_011525544.1:n.864-139_864-137delinsCAG
NM_000660.6:c.861-139_861-137delinsCAG	NP_000651.3:n.861-139_861-137delinsCAG
XM_011527242.2:c.864-139_864-137delinsCAG	XP_011525544.1:n.864-139_864-137delinsCAG
NM_000660.7:c.861-139_861-137delinsCAG MANE Select	NP_000651.3:n.861-139_861-137delinsCAG