Canonical Allele Identifier: CA2585296549

Gene: TGFB1

Linked Data

• gnomAD v4: 19-41342391-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41342392_41342393insAT , CM000681.2:g.41342392_41342393insAT	GRCh38
NC_000019.9:g.41848297_41848298insAT , CM000681.1:g.41848297_41848298insAT	GRCh37
NC_000019.8:g.46540137_46540138insAT	NCBI36
NG_013364.1:g.16535_16536insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.635-145_635-144insTA MANE Select	ENSP00000221930.4:n.635-145_635-144insTA
ENST00000600196.2:c.635-145_635-144insTA	ENSP00000504008.1:n.635-145_635-144insTA
ENST00000677934.1:c.634+2355_634+2356insTA	ENSP00000504769.1:n.634+2355_634+2356insTA
ENST00000221930.5:c.635-145_635-144insTA	ENSP00000221930.4:n.635-145_635-144insTA
ENST00000597453.1:n.166-145_166-144insTA
ENST00000600196.1:n.95-145_95-144insTA
NM_000660.5:c.635-145_635-144insTA	NP_000651.3:n.635-145_635-144insTA
XM_011527242.1:c.635-145_635-144insTA	XP_011525544.1:n.635-145_635-144insTA
NM_000660.6:c.635-145_635-144insTA	NP_000651.3:n.635-145_635-144insTA
XM_011527242.2:c.635-145_635-144insTA	XP_011525544.1:n.635-145_635-144insTA
NM_000660.7:c.635-145_635-144insTA MANE Select	NP_000651.3:n.635-145_635-144insTA