Canonical Allele Identifier: CA2336426100

Gene: TGFB1 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41352779G= , CM000681.2:g.41352779G=	GRCh38
NC_000019.9:g.41858684G= , CM000681.1:g.41858684G=	GRCh37
NC_000019.8:g.46550524G=	NCBI36
NG_013091.1:g.16395C=
NG_013364.1:g.6148C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.266C= (TGFB1) MANE Select	ENSP00000221930.4:p.Ala89=
ENST00000600196.2:c.266C= (TGFB1)	ENSP00000504008.1:p.Ala89=
ENST00000677934.1:c.266C= (TGFB1)	ENSP00000504769.1:p.Ala89=
ENST00000221930.5:c.266C= (TGFB1)	ENSP00000221930.4:p.Ala89=
ENST00000539627.5:c.-30+1577G= (TMEM91)	ENSP00000441900.1:n.-30+1577G=
ENST00000604424.1:n.350+1577G=
NM_000660.5:c.266C= (TGFB1)	NP_000651.3:p.Ala89=
XM_011527242.1:c.266C= (TGFB1)	XP_011525544.1:p.Ala89=
NM_000660.6:c.266C= (TGFB1)	NP_000651.3:p.Ala89=
XM_011527242.2:c.266C= (TGFB1)	XP_011525544.1:p.Ala89=
NM_000660.7:c.266C= (TGFB1) MANE Select	NP_000651.3:p.Ala89=