Canonical Allele Identifier: CA2336426198

Gene: TGFB1 TMEM91

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41352981T= , CM000681.2:g.41352981T=	GRCh38
NC_000019.9:g.41858886T= , CM000681.1:g.41858886T=	GRCh37
NC_000019.8:g.46550726T=	NCBI36
NG_013091.1:g.16193A=
NG_013364.1:g.5946A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.64A= (TGFB1) MANE Select	ENSP00000221930.4:p.Thr22=
ENST00000600196.2:c.64A= (TGFB1)	ENSP00000504008.1:p.Thr22=
ENST00000677934.1:c.64A= (TGFB1)	ENSP00000504769.1:p.Thr22=
ENST00000221930.5:c.64A= (TGFB1)	ENSP00000221930.4:p.Thr22=
ENST00000539627.5:c.-30+1779T= (TMEM91)	ENSP00000441900.1:n.-30+1779T=
ENST00000604424.1:n.350+1779T=
NM_000660.5:c.64A= (TGFB1)	NP_000651.3:p.Thr22=
XM_011527242.1:c.64A= (TGFB1)	XP_011525544.1:p.Thr22=
NM_000660.6:c.64A= (TGFB1)	NP_000651.3:p.Thr22=
XM_011527242.2:c.64A= (TGFB1)	XP_011525544.1:p.Thr22=
NM_000660.7:c.64A= (TGFB1) MANE Select	NP_000651.3:p.Thr22=