Canonical Allele Identifier: CA1354873977
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30674092_30674093delinsGT , CM000665.2:g.30674092_30674093delinsGT GRCh38
NC_000003.11:g.30715584_30715585delinsGT , CM000665.1:g.30715584_30715585delinsGT GRCh37
NC_000003.10:g.30690588_30690589delinsGT NCBI36
NG_007490.1:g.72591_72592delinsGT , LRG_779:g.72591_72592delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1255-13_1255-12delinsGT MANE Select ENSP00000295754.5:n.1255-13_1255-12delinsGT
ENST00000672866.1:n.2851-13_2851-12delinsGT
ENST00000673203.1:n.120_121delinsGT
ENST00000295754.9:c.1255-13_1255-12delinsGT ENSP00000295754.5:n.1255-13_1255-12delinsGT
ENST00000359013.4:c.1330-13_1330-12delinsGT ENSP00000351905.4:n.1330-13_1330-12delinsGT
NM_001024847.2:c.1330-13_1330-12delinsGT , LRG_779t1:c.1330-13_1330-12delinsGT NP_001020018.1:n.1330-13_1330-12delinsGT
NM_003242.5:c.1255-13_1255-12delinsGT NP_003233.4:n.1255-13_1255-12delinsGT
XM_011534043.1:c.1282-13_1282-12delinsGT XP_011532345.1:n.1282-13_1282-12delinsGT
XM_011534044.1:c.1207-13_1207-12delinsGT XP_011532346.1:n.1207-13_1207-12delinsGT
XM_011534045.1:c.1150-13_1150-12delinsGT XP_011532347.1:n.1150-13_1150-12delinsGT
XM_011534043.2:c.1282-13_1282-12delinsGT XP_011532345.1:n.1282-13_1282-12delinsGT
XM_011534045.3:c.1150-13_1150-12delinsGT XP_011532347.1:n.1150-13_1150-12delinsGT
XM_017007106.1:c.1150-13_1150-12delinsGT XP_016862595.1:n.1150-13_1150-12delinsGT
NM_003242.6:c.1255-13_1255-12delinsGT MANE Select NP_003233.4:n.1255-13_1255-12delinsGT