Canonical Allele Identifier: CA2336420960
Gene: TGFB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41341859_41341863delinsCTCCA , CM000681.2:g.41341859_41341863delinsCTCCA GRCh38
NC_000019.9:g.41847764_41847768delinsCTCCA , CM000681.1:g.41847764_41847768delinsCTCCA GRCh37
NC_000019.8:g.46539604_46539608delinsCTCCA NCBI36
NG_013364.1:g.17064_17068delinsTGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000221930.6:c.860+20_860+24delinsTGGAG MANE Select ENSP00000221930.4:n.860+20_860+24delinsTGGAG
ENST00000600196.2:c.712+307_712+311delinsTGGAG ENSP00000504008.1:n.712+307_712+311delinsTGGAG
ENST00000677934.1:c.634+2884_634+2888delinsTGGAG ENSP00000504769.1:n.634+2884_634+2888delinsTGGAG
ENST00000221930.5:c.860+20_860+24delinsTGGAG ENSP00000221930.4:n.860+20_860+24delinsTGGAG
ENST00000598758.5:c.148+20_148+24delinsTGGAG
ENST00000600196.1:n.172+307_172+311delinsTGGAG
NM_000660.5:c.860+20_860+24delinsTGGAG NP_000651.3:n.860+20_860+24delinsTGGAG
XM_011527242.1:c.863+20_863+24delinsTGGAG XP_011525544.1:n.863+20_863+24delinsTGGAG
NM_000660.6:c.860+20_860+24delinsTGGAG NP_000651.3:n.860+20_860+24delinsTGGAG
XM_011527242.2:c.863+20_863+24delinsTGGAG XP_011525544.1:n.863+20_863+24delinsTGGAG
NM_000660.7:c.860+20_860+24delinsTGGAG MANE Select NP_000651.3:n.860+20_860+24delinsTGGAG