Canonical Allele Identifier: CA2336421236

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342407_41342414delinsTTTTTTTG , CM000681.2:g.41342407_41342414delinsTTTTTTTG	GRCh38
NC_000019.9:g.41848312_41848319delinsTTTTTTTG , CM000681.1:g.41848312_41848319delinsTTTTTTTG	GRCh37
NC_000019.8:g.46540152_46540159delinsTTTTTTTG	NCBI36
NG_013364.1:g.16513_16520delinsCAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-167_635-160delinsCAAAAAAA MANE Select	ENSP00000221930.4:n.635-167_635-160delinsCAAAAAAA
ENST00000600196.2:c.635-167_635-160delinsCAAAAAAA	ENSP00000504008.1:n.635-167_635-160delinsCAAAAAAA
ENST00000677934.1:c.634+2333_634+2340delinsCAAAAAAA	ENSP00000504769.1:n.634+2333_634+2340delinsCAAAAAAA
ENST00000221930.5:c.635-167_635-160delinsCAAAAAAA	ENSP00000221930.4:n.635-167_635-160delinsCAAAAAAA
ENST00000597453.1:n.166-167_166-160delinsCAAAAAAA
ENST00000600196.1:n.95-167_95-160delinsCAAAAAAA
NM_000660.5:c.635-167_635-160delinsCAAAAAAA	NP_000651.3:n.635-167_635-160delinsCAAAAAAA
XM_011527242.1:c.635-167_635-160delinsCAAAAAAA	XP_011525544.1:n.635-167_635-160delinsCAAAAAAA
NM_000660.6:c.635-167_635-160delinsCAAAAAAA	NP_000651.3:n.635-167_635-160delinsCAAAAAAA
XM_011527242.2:c.635-167_635-160delinsCAAAAAAA	XP_011525544.1:n.635-167_635-160delinsCAAAAAAA
NM_000660.7:c.635-167_635-160delinsCAAAAAAA MANE Select	NP_000651.3:n.635-167_635-160delinsCAAAAAAA