Canonical Allele Identifier: CA2336423740

Gene: TGFB1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41347908_41347909delinsTG , CM000681.2:g.41347908_41347909delinsTG	GRCh38
NC_000019.9:g.41853813_41853814delinsTG , CM000681.1:g.41853813_41853814delinsTG	GRCh37
NC_000019.8:g.46545653_46545654delinsTG	NCBI36
NG_013364.1:g.11018_11019delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221930.6:c.516+386_516+387delinsCA MANE Select	ENSP00000221930.4:n.516+386_516+387delinsCA
ENST00000600196.2:c.516+386_516+387delinsCA	ENSP00000504008.1:n.516+386_516+387delinsCA
ENST00000677934.1:c.516+386_516+387delinsCA	ENSP00000504769.1:n.516+386_516+387delinsCA
ENST00000221930.5:c.516+386_516+387delinsCA	ENSP00000221930.4:n.516+386_516+387delinsCA
ENST00000597453.1:n.47+386_47+387delinsCA
NM_000660.5:c.516+386_516+387delinsCA	NP_000651.3:n.516+386_516+387delinsCA
XM_011527242.1:c.516+386_516+387delinsCA	XP_011525544.1:n.516+386_516+387delinsCA
NM_000660.6:c.516+386_516+387delinsCA	NP_000651.3:n.516+386_516+387delinsCA
XM_011527242.2:c.516+386_516+387delinsCA	XP_011525544.1:n.516+386_516+387delinsCA
NM_000660.7:c.516+386_516+387delinsCA MANE Select	NP_000651.3:n.516+386_516+387delinsCA