Canonical Allele Identifier: CA308518939
Gene: TGFB1 HGNC NCBI
TMEM91 HGNC NCBI

Linked Data

dbSNP Id: rs200016578

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41353162_41353163insGGG , CM000681.2:g.41353162_41353163insGGG GRCh38
NC_000019.9:g.41859067_41859068insGGG , CM000681.1:g.41859067_41859068insGGG GRCh37
NC_000019.8:g.46550907_46550908insGGG NCBI36
NG_013091.1:g.16011_16012insCCC
NG_013364.1:g.5764_5765insCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.-119_-118insCCC (TGFB1) MANE Select ENSP00000221930.4:n.-119_-118insCCC
ENST00000221930.5:c.-119_-118insCCC (TGFB1) ENSP00000221930.4:n.-119_-118insCCC
ENST00000539627.5:c.-30+1960_-30+1961insGGG (TMEM91) ENSP00000441900.1:n.-30+1960_-30+1961insGGG
ENST00000604424.1:n.350+1960_350+1961insGGG
NM_000660.5:c.-119_-118insCCC (TGFB1) NP_000651.3:n.-119_-118insCCC
XM_011527242.1:c.-119_-118insCCC (TGFB1) XP_011525544.1:n.-119_-118insCCC
NM_000660.6:c.-119_-118insCCC (TGFB1) NP_000651.3:n.-119_-118insCCC
XM_011527242.2:c.-119_-118insCCC (TGFB1) XP_011525544.1:n.-119_-118insCCC
NM_000660.7:c.-119_-118insCCC (TGFB1) MANE Select NP_000651.3:n.-119_-118insCCC