Canonical Allele Identifier: CA2336421221

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342388_41342393delinsCTCTTT , CM000681.2:g.41342388_41342393delinsCTCTTT	GRCh38
NC_000019.9:g.41848293_41848298delinsCTCTTT , CM000681.1:g.41848293_41848298delinsCTCTTT	GRCh37
NC_000019.8:g.46540133_46540138delinsCTCTTT	NCBI36
NG_013364.1:g.16534_16539delinsAAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-146_635-141delinsAAAGAG MANE Select	ENSP00000221930.4:n.635-146_635-141delinsAAAGAG
ENST00000600196.2:c.635-146_635-141delinsAAAGAG	ENSP00000504008.1:n.635-146_635-141delinsAAAGAG
ENST00000677934.1:c.634+2354_634+2359delinsAAAGAG	ENSP00000504769.1:n.634+2354_634+2359delinsAAAGAG
ENST00000221930.5:c.635-146_635-141delinsAAAGAG	ENSP00000221930.4:n.635-146_635-141delinsAAAGAG
ENST00000597453.1:n.166-146_166-141delinsAAAGAG
ENST00000600196.1:n.95-146_95-141delinsAAAGAG
NM_000660.5:c.635-146_635-141delinsAAAGAG	NP_000651.3:n.635-146_635-141delinsAAAGAG
XM_011527242.1:c.635-146_635-141delinsAAAGAG	XP_011525544.1:n.635-146_635-141delinsAAAGAG
NM_000660.6:c.635-146_635-141delinsAAAGAG	NP_000651.3:n.635-146_635-141delinsAAAGAG
XM_011527242.2:c.635-146_635-141delinsAAAGAG	XP_011525544.1:n.635-146_635-141delinsAAAGAG
NM_000660.7:c.635-146_635-141delinsAAAGAG MANE Select	NP_000651.3:n.635-146_635-141delinsAAAGAG