Canonical Allele Identifier: CA2849098762

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348083_41348084insATTGC , CM000681.2:g.41348083_41348084insATTGC	GRCh38
NC_000019.9:g.41853988_41853989insATTGC , CM000681.1:g.41853988_41853989insATTGC	GRCh37
NC_000019.8:g.46545828_46545829insATTGC	NCBI36
NG_013364.1:g.10843_10844insGCAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.516+211_516+212insGCAAT MANE Select	ENSP00000221930.4:n.516+211_516+212insGCAAT
ENST00000600196.2:c.516+211_516+212insGCAAT	ENSP00000504008.1:n.516+211_516+212insGCAAT
ENST00000677934.1:c.516+211_516+212insGCAAT	ENSP00000504769.1:n.516+211_516+212insGCAAT
ENST00000221930.5:c.516+211_516+212insGCAAT	ENSP00000221930.4:n.516+211_516+212insGCAAT
ENST00000597453.1:n.47+211_47+212insGCAAT
NM_000660.5:c.516+211_516+212insGCAAT	NP_000651.3:n.516+211_516+212insGCAAT
XM_011527242.1:c.516+211_516+212insGCAAT	XP_011525544.1:n.516+211_516+212insGCAAT
NM_000660.6:c.516+211_516+212insGCAAT	NP_000651.3:n.516+211_516+212insGCAAT
XM_011527242.2:c.516+211_516+212insGCAAT	XP_011525544.1:n.516+211_516+212insGCAAT
NM_000660.7:c.516+211_516+212insGCAAT MANE Select	NP_000651.3:n.516+211_516+212insGCAAT