Canonical Allele Identifier: CA2585297341

Gene: TGFB1 TMEM91

Linked Data

• gnomAD v4: 19-41352662-C-CCCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41352664_41352665insCTCC , CM000681.2:g.41352664_41352665insCTCC	GRCh38
NC_000019.9:g.41858569_41858570insCTCC , CM000681.1:g.41858569_41858570insCTCC	GRCh37
NC_000019.8:g.46550409_46550410insCTCC	NCBI36
NG_013091.1:g.16511_16512insAGGG
NG_013364.1:g.6264_6265insAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.355+27_355+28insAGGG (TGFB1) MANE Select	ENSP00000221930.4:n.355+27_355+28insAGGG
ENST00000600196.2:c.355+27_355+28insAGGG (TGFB1)	ENSP00000504008.1:n.355+27_355+28insAGGG
ENST00000677934.1:c.355+27_355+28insAGGG (TGFB1)	ENSP00000504769.1:n.355+27_355+28insAGGG
ENST00000221930.5:c.355+27_355+28insAGGG (TGFB1)	ENSP00000221930.4:n.355+27_355+28insAGGG
ENST00000539627.5:c.-30+1462_-30+1463insCTCC (TMEM91)	ENSP00000441900.1:n.-30+1462_-30+1463insCTCC
ENST00000604424.1:n.350+1462_350+1463insCTCC
NM_000660.5:c.355+27_355+28insAGGG (TGFB1)	NP_000651.3:n.355+27_355+28insAGGG
XM_011527242.1:c.355+27_355+28insAGGG (TGFB1)	XP_011525544.1:n.355+27_355+28insAGGG
NM_000660.6:c.355+27_355+28insAGGG (TGFB1)	NP_000651.3:n.355+27_355+28insAGGG
XM_011527242.2:c.355+27_355+28insAGGG (TGFB1)	XP_011525544.1:n.355+27_355+28insAGGG
NM_000660.7:c.355+27_355+28insAGGG (TGFB1) MANE Select	NP_000651.3:n.355+27_355+28insAGGG