Canonical Allele Identifier: CA2336421242

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342412_41342414delinsTTG , CM000681.2:g.41342412_41342414delinsTTG	GRCh38
NC_000019.9:g.41848317_41848319delinsTTG , CM000681.1:g.41848317_41848319delinsTTG	GRCh37
NC_000019.8:g.46540157_46540159delinsTTG	NCBI36
NG_013364.1:g.16513_16515delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-167_635-165delinsCAA MANE Select	ENSP00000221930.4:n.635-167_635-165delinsCAA
ENST00000600196.2:c.635-167_635-165delinsCAA	ENSP00000504008.1:n.635-167_635-165delinsCAA
ENST00000677934.1:c.634+2333_634+2335delinsCAA	ENSP00000504769.1:n.634+2333_634+2335delinsCAA
ENST00000221930.5:c.635-167_635-165delinsCAA	ENSP00000221930.4:n.635-167_635-165delinsCAA
ENST00000597453.1:n.166-167_166-165delinsCAA
ENST00000600196.1:n.95-167_95-165delinsCAA
NM_000660.5:c.635-167_635-165delinsCAA	NP_000651.3:n.635-167_635-165delinsCAA
XM_011527242.1:c.635-167_635-165delinsCAA	XP_011525544.1:n.635-167_635-165delinsCAA
NM_000660.6:c.635-167_635-165delinsCAA	NP_000651.3:n.635-167_635-165delinsCAA
XM_011527242.2:c.635-167_635-165delinsCAA	XP_011525544.1:n.635-167_635-165delinsCAA
NM_000660.7:c.635-167_635-165delinsCAA MANE Select	NP_000651.3:n.635-167_635-165delinsCAA