Canonical Allele Identifier: CA2814428769

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341860_41341862del , CM000681.2:g.41341860_41341862del	GRCh38
NC_000019.9:g.41847765_41847767del , CM000681.1:g.41847765_41847767del	GRCh37
NC_000019.8:g.46539605_46539607del	NCBI36
NG_013364.1:g.17067_17069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.860+23_860+25del MANE Select	ENSP00000221930.4:n.860+23_860+25del
ENST00000600196.2:c.712+310_712+312del	ENSP00000504008.1:n.712+310_712+312del
ENST00000677934.1:c.634+2887_634+2889del	ENSP00000504769.1:n.634+2887_634+2889del
ENST00000221930.5:c.860+23_860+25del	ENSP00000221930.4:n.860+23_860+25del
ENST00000598758.5:c.148+23_148+25del
ENST00000600196.1:n.172+310_172+312del
NM_000660.5:c.860+23_860+25del	NP_000651.3:n.860+23_860+25del
XM_011527242.1:c.863+23_863+25del	XP_011525544.1:n.863+23_863+25del
NM_000660.6:c.860+23_860+25del	NP_000651.3:n.860+23_860+25del
XM_011527242.2:c.863+23_863+25del	XP_011525544.1:n.863+23_863+25del
NM_000660.7:c.860+23_860+25del MANE Select	NP_000651.3:n.860+23_860+25del