Canonical Allele Identifier: CA2336425196
Community Standard Title: NM_000660.7(TGFB1):c.355+1709T=
Gene: TGFB1 HGNC NCBI
TMEM91 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41350981A= , CM000681.2:g.41350981A= GRCh38
NC_000019.9:g.41856886A= , CM000681.1:g.41856886A= GRCh37
NC_000019.8:g.46548726A= NCBI36
NG_013364.1:g.7946T=

Transcript Alleles

HGVS Amino-acid Change
NM_000660.7:c.355+1709T= (TGFB1) MANE Select NP_000651.3:n.355+1709T=
ENST00000221930.6:c.355+1709T= (TGFB1) MANE Select ENSP00000221930.4:n.355+1709T=
NM_000660.5:c.355+1709T= (TGFB1) NP_000651.3:n.355+1709T=
NM_000660.6:c.355+1709T= (TGFB1) NP_000651.3:n.355+1709T=
ENST00000221930.5:c.355+1709T= (TGFB1) ENSP00000221930.4:n.355+1709T=
ENST00000539627.5:c.-251A= (TMEM91) ENSP00000441900.1:n.-251A=
ENST00000600196.2:c.355+1709T= (TGFB1) ENSP00000504008.1:n.355+1709T=
ENST00000604424.1:n.129A=
ENST00000677934.1:c.355+1709T= (TGFB1) ENSP00000504769.1:n.355+1709T=
XM_011527242.1:c.355+1709T= (TGFB1) XP_011525544.1:n.355+1709T=
XM_011527242.2:c.355+1709T= (TGFB1) XP_011525544.1:n.355+1709T=