Canonical Allele Identifier: CA2336423853

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41348129_41348130delinsTC , CM000681.2:g.41348129_41348130delinsTC	GRCh38
NC_000019.9:g.41854034_41854035delinsTC , CM000681.1:g.41854034_41854035delinsTC	GRCh37
NC_000019.8:g.46545874_46545875delinsTC	NCBI36
NG_013364.1:g.10797_10798delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.516+165_516+166delinsGA MANE Select	ENSP00000221930.4:n.516+165_516+166delinsGA
ENST00000600196.2:c.516+165_516+166delinsGA	ENSP00000504008.1:n.516+165_516+166delinsGA
ENST00000677934.1:c.516+165_516+166delinsGA	ENSP00000504769.1:n.516+165_516+166delinsGA
ENST00000221930.5:c.516+165_516+166delinsGA	ENSP00000221930.4:n.516+165_516+166delinsGA
ENST00000597453.1:n.47+165_47+166delinsGA
NM_000660.5:c.516+165_516+166delinsGA	NP_000651.3:n.516+165_516+166delinsGA
XM_011527242.1:c.516+165_516+166delinsGA	XP_011525544.1:n.516+165_516+166delinsGA
NM_000660.6:c.516+165_516+166delinsGA	NP_000651.3:n.516+165_516+166delinsGA
XM_011527242.2:c.516+165_516+166delinsGA	XP_011525544.1:n.516+165_516+166delinsGA
NM_000660.7:c.516+165_516+166delinsGA MANE Select	NP_000651.3:n.516+165_516+166delinsGA