Canonical Allele Identifier: CA2336426332

Gene: TGFB1 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41353212_41353213delinsAC , CM000681.2:g.41353212_41353213delinsAC	GRCh38
NC_000019.9:g.41859117_41859118delinsAC , CM000681.1:g.41859117_41859118delinsAC	GRCh37
NC_000019.8:g.46550957_46550958delinsAC	NCBI36
NG_013091.1:g.15961_15962delinsGT
NG_013364.1:g.5714_5715delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.-169_-168delinsGT (TGFB1) MANE Select	ENSP00000221930.4:n.-169_-168delinsGT
ENST00000221930.5:c.-169_-168delinsGT (TGFB1)	ENSP00000221930.4:n.-169_-168delinsGT
ENST00000539627.5:c.-30+2010_-30+2011delinsAC (TMEM91)	ENSP00000441900.1:n.-30+2010_-30+2011delinsAC
ENST00000604424.1:n.350+2010_350+2011delinsAC
NM_000660.5:c.-169_-168delinsGT (TGFB1)	NP_000651.3:n.-169_-168delinsGT
XM_011527242.1:c.-169_-168delinsGT (TGFB1)	XP_011525544.1:n.-169_-168delinsGT
NM_000660.6:c.-169_-168delinsGT (TGFB1)	NP_000651.3:n.-169_-168delinsGT
XM_011527242.2:c.-169_-168delinsGT (TGFB1)	XP_011525544.1:n.-169_-168delinsGT
NM_000660.7:c.-169_-168delinsGT (TGFB1) MANE Select	NP_000651.3:n.-169_-168delinsGT