Canonical Allele Identifier: CA2336423864

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348144_41348147delinsAAGC , CM000681.2:g.41348144_41348147delinsAAGC	GRCh38
NC_000019.9:g.41854049_41854052delinsAAGC , CM000681.1:g.41854049_41854052delinsAAGC	GRCh37
NC_000019.8:g.46545889_46545892delinsAAGC	NCBI36
NG_013364.1:g.10780_10783delinsGCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.516+148_516+151delinsGCTT MANE Select	ENSP00000221930.4:n.516+148_516+151delinsGCTT
ENST00000600196.2:c.516+148_516+151delinsGCTT	ENSP00000504008.1:n.516+148_516+151delinsGCTT
ENST00000677934.1:c.516+148_516+151delinsGCTT	ENSP00000504769.1:n.516+148_516+151delinsGCTT
ENST00000221930.5:c.516+148_516+151delinsGCTT	ENSP00000221930.4:n.516+148_516+151delinsGCTT
ENST00000597453.1:n.47+148_47+151delinsGCTT
NM_000660.5:c.516+148_516+151delinsGCTT	NP_000651.3:n.516+148_516+151delinsGCTT
XM_011527242.1:c.516+148_516+151delinsGCTT	XP_011525544.1:n.516+148_516+151delinsGCTT
NM_000660.6:c.516+148_516+151delinsGCTT	NP_000651.3:n.516+148_516+151delinsGCTT
XM_011527242.2:c.516+148_516+151delinsGCTT	XP_011525544.1:n.516+148_516+151delinsGCTT
NM_000660.7:c.516+148_516+151delinsGCTT MANE Select	NP_000651.3:n.516+148_516+151delinsGCTT