Canonical Allele Identifier: CA308515020

Gene: TGFB1

Linked Data

• dbSNP Id: rs386809353

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41347991_41348001delinsCA , CM000681.2:g.41347991_41348001delinsCA	GRCh38
NC_000019.9:g.41853896_41853906delinsCA , CM000681.1:g.41853896_41853906delinsCA	GRCh37
NC_000019.8:g.46545736_46545746delinsCA	NCBI36
NG_013364.1:g.10926_10936delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.516+294_516+304delinsTG MANE Select	ENSP00000221930.4:n.516+294_516+304delinsTG
ENST00000600196.2:c.516+294_516+304delinsTG	ENSP00000504008.1:n.516+294_516+304delinsTG
ENST00000677934.1:c.516+294_516+304delinsTG	ENSP00000504769.1:n.516+294_516+304delinsTG
ENST00000221930.5:c.516+294_516+304delinsTG	ENSP00000221930.4:n.516+294_516+304delinsTG
ENST00000597453.1:n.47+294_47+304delinsTG
NM_000660.5:c.516+294_516+304delinsTG	NP_000651.3:n.516+294_516+304delinsTG
XM_011527242.1:c.516+294_516+304delinsTG	XP_011525544.1:n.516+294_516+304delinsTG
NM_000660.6:c.516+294_516+304delinsTG	NP_000651.3:n.516+294_516+304delinsTG
XM_011527242.2:c.516+294_516+304delinsTG	XP_011525544.1:n.516+294_516+304delinsTG
NM_000660.7:c.516+294_516+304delinsTG MANE Select	NP_000651.3:n.516+294_516+304delinsTG