Canonical Allele Identifier: CA2336426321

Gene: TGFB1 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41353184_41353185delinsAG , CM000681.2:g.41353184_41353185delinsAG	GRCh38
NC_000019.9:g.41859089_41859090delinsAG , CM000681.1:g.41859089_41859090delinsAG	GRCh37
NC_000019.8:g.46550929_46550930delinsAG	NCBI36
NG_013091.1:g.15989_15990delinsCT
NG_013364.1:g.5742_5743delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.-141_-140delinsCT (TGFB1) MANE Select	ENSP00000221930.4:n.-141_-140delinsCT
ENST00000221930.5:c.-141_-140delinsCT (TGFB1)	ENSP00000221930.4:n.-141_-140delinsCT
ENST00000539627.5:c.-30+1982_-30+1983delinsAG (TMEM91)	ENSP00000441900.1:n.-30+1982_-30+1983delinsAG
ENST00000604424.1:n.350+1982_350+1983delinsAG
NM_000660.5:c.-141_-140delinsCT (TGFB1)	NP_000651.3:n.-141_-140delinsCT
XM_011527242.1:c.-141_-140delinsCT (TGFB1)	XP_011525544.1:n.-141_-140delinsCT
NM_000660.6:c.-141_-140delinsCT (TGFB1)	NP_000651.3:n.-141_-140delinsCT
XM_011527242.2:c.-141_-140delinsCT (TGFB1)	XP_011525544.1:n.-141_-140delinsCT
NM_000660.7:c.-141_-140delinsCT (TGFB1) MANE Select	NP_000651.3:n.-141_-140delinsCT