Canonical Allele Identifier: CA2336416588

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41332497_41332501delinsATAAT , CM000681.2:g.41332497_41332501delinsATAAT	GRCh38
NC_000019.9:g.41838402_41838406delinsATAAT , CM000681.1:g.41838402_41838406delinsATAAT	GRCh37
NC_000019.8:g.46530242_46530246delinsATAAT	NCBI36
NG_013364.1:g.26426_26430delinsATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.861-220_861-216delinsATTAT MANE Select	ENSP00000221930.4:n.861-220_861-216delinsATTAT
ENST00000600196.2:c.713-220_713-216delinsATTAT	ENSP00000504008.1:n.713-220_713-216delinsATTAT
ENST00000677934.1:c.635-220_635-216delinsATTAT	ENSP00000504769.1:n.635-220_635-216delinsATTAT
ENST00000221930.5:c.861-220_861-216delinsATTAT	ENSP00000221930.4:n.861-220_861-216delinsATTAT
ENST00000598758.5:c.149-220_149-216delinsATTAT
ENST00000600196.1:n.173-220_173-216delinsATTAT
NM_000660.5:c.861-220_861-216delinsATTAT	NP_000651.3:n.861-220_861-216delinsATTAT
XM_011527242.1:c.864-220_864-216delinsATTAT	XP_011525544.1:n.864-220_864-216delinsATTAT
NM_000660.6:c.861-220_861-216delinsATTAT	NP_000651.3:n.861-220_861-216delinsATTAT
XM_011527242.2:c.864-220_864-216delinsATTAT	XP_011525544.1:n.864-220_864-216delinsATTAT
NM_000660.7:c.861-220_861-216delinsATTAT MANE Select	NP_000651.3:n.861-220_861-216delinsATTAT