Canonical Allele Identifier: CA2576793242

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41341861_41341863del , CM000681.2:g.41341861_41341863del	GRCh38
NC_000019.9:g.41847766_41847768del , CM000681.1:g.41847766_41847768del	GRCh37
NC_000019.8:g.46539606_46539608del	NCBI36
NG_013364.1:g.17064_17066del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.860+20_860+22del MANE Select	ENSP00000221930.4:n.860+20_860+22del
ENST00000600196.2:c.712+307_712+309del	ENSP00000504008.1:n.712+307_712+309del
ENST00000677934.1:c.634+2884_634+2886del	ENSP00000504769.1:n.634+2884_634+2886del
ENST00000221930.5:c.860+20_860+22del	ENSP00000221930.4:n.860+20_860+22del
ENST00000598758.5:c.148+20_148+22del
ENST00000600196.1:n.172+307_172+309del
NM_000660.5:c.860+20_860+22del	NP_000651.3:n.860+20_860+22del
XM_011527242.1:c.863+20_863+22del	XP_011525544.1:n.863+20_863+22del
NM_000660.6:c.860+20_860+22del	NP_000651.3:n.860+20_860+22del
XM_011527242.2:c.863+20_863+22del	XP_011525544.1:n.863+20_863+22del
NM_000660.7:c.860+20_860+22del MANE Select	NP_000651.3:n.860+20_860+22del