Canonical Allele Identifier: CA2336421246

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342413_41342415delinsTGA , CM000681.2:g.41342413_41342415delinsTGA	GRCh38
NC_000019.9:g.41848318_41848320delinsTGA , CM000681.1:g.41848318_41848320delinsTGA	GRCh37
NC_000019.8:g.46540158_46540160delinsTGA	NCBI36
NG_013364.1:g.16512_16514delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-168_635-166delinsTCA MANE Select	ENSP00000221930.4:n.635-168_635-166delinsTCA
ENST00000600196.2:c.635-168_635-166delinsTCA	ENSP00000504008.1:n.635-168_635-166delinsTCA
ENST00000677934.1:c.634+2332_634+2334delinsTCA	ENSP00000504769.1:n.634+2332_634+2334delinsTCA
ENST00000221930.5:c.635-168_635-166delinsTCA	ENSP00000221930.4:n.635-168_635-166delinsTCA
ENST00000597453.1:n.166-168_166-166delinsTCA
ENST00000600196.1:n.95-168_95-166delinsTCA
NM_000660.5:c.635-168_635-166delinsTCA	NP_000651.3:n.635-168_635-166delinsTCA
XM_011527242.1:c.635-168_635-166delinsTCA	XP_011525544.1:n.635-168_635-166delinsTCA
NM_000660.6:c.635-168_635-166delinsTCA	NP_000651.3:n.635-168_635-166delinsTCA
XM_011527242.2:c.635-168_635-166delinsTCA	XP_011525544.1:n.635-168_635-166delinsTCA
NM_000660.7:c.635-168_635-166delinsTCA MANE Select	NP_000651.3:n.635-168_635-166delinsTCA