Canonical Allele Identifier: CA2573050377

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348130_41348131delinsCA , CM000681.2:g.41348130_41348131delinsCA	GRCh38
NC_000019.9:g.41854035_41854036delinsCA , CM000681.1:g.41854035_41854036delinsCA	GRCh37
NC_000019.8:g.46545875_46545876delinsCA	NCBI36
NG_013364.1:g.10796_10797delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000221930.6:c.516+164_516+165delinsTG MANE Select	ENSP00000221930.4:n.516+164_516+165delins...
ENST00000600196.2:c.516+164_516+165delinsTG	ENSP00000504008.1:n.516+164_516+165delins...
ENST00000677934.1:c.516+164_516+165delinsTG	ENSP00000504769.1:n.516+164_516+165delins...
ENST00000221930.5:c.516+164_516+165delinsTG	ENSP00000221930.4:n.516+164_516+165delins...
ENST00000597453.1:n.47+164_47+165delinsTG
NM_000660.5:c.516+164_516+165delinsTG	NP_000651.3:n.516+164_516+165delinsTG
XM_011527242.1:c.516+164_516+165delinsTG	XP_011525544.1:n.516+164_516+165delinsTG
NM_000660.6:c.516+164_516+165delinsTG	NP_000651.3:n.516+164_516+165delinsTG
XM_011527242.2:c.516+164_516+165delinsTG	XP_011525544.1:n.516+164_516+165delinsTG
NM_000660.7:c.516+164_516+165delinsTG MANE Select	NP_000651.3:n.516+164_516+165delinsTG