Canonical Allele Identifier: CA1354881638

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691406_30691407delinsCT , CM000665.2:g.30691406_30691407delinsCT	GRCh38
NC_000003.11:g.30732898_30732899delinsCT , CM000665.1:g.30732898_30732899delinsCT	GRCh37
NC_000003.10:g.30707902_30707903delinsCT	NCBI36
NG_007490.1:g.89905_89906delinsCT , LRG_779:g.89905_89906delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1525-14_1525-13delinsCT MANE Select	ENSP00000295754.5:n.1525-14_1525-13delinsCT
ENST00000672050.1:n.409-14_409-13delinsCT
ENST00000672866.1:n.3121-14_3121-13delinsCT
ENST00000673203.1:n.403-14_403-13delinsCT
ENST00000295754.9:c.1525-14_1525-13delinsCT	ENSP00000295754.5:n.1525-14_1525-13delinsCT
ENST00000359013.4:c.1600-14_1600-13delinsCT	ENSP00000351905.4:n.1600-14_1600-13delinsCT
NM_001024847.2:c.1600-14_1600-13delinsCT , LRG_779t1:c.1600-14_1600-13delinsCT	NP_001020018.1:n.1600-14_1600-13delinsCT
NM_003242.5:c.1525-14_1525-13delinsCT	NP_003233.4:n.1525-14_1525-13delinsCT
XM_011534043.1:c.1552-14_1552-13delinsCT	XP_011532345.1:n.1552-14_1552-13delinsCT
XM_011534044.1:c.1477-14_1477-13delinsCT	XP_011532346.1:n.1477-14_1477-13delinsCT
XM_011534045.1:c.1420-14_1420-13delinsCT	XP_011532347.1:n.1420-14_1420-13delinsCT
XM_011534043.2:c.1552-14_1552-13delinsCT	XP_011532345.1:n.1552-14_1552-13delinsCT
XM_011534045.3:c.1420-14_1420-13delinsCT	XP_011532347.1:n.1420-14_1420-13delinsCT
XM_017007106.1:c.1420-14_1420-13delinsCT	XP_016862595.1:n.1420-14_1420-13delinsCT
NM_003242.6:c.1525-14_1525-13delinsCT MANE Select	NP_003233.4:n.1525-14_1525-13delinsCT