Canonical Allele Identifier: CA1354874050
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30674265_30674268delinsCATT , CM000665.2:g.30674265_30674268delinsCATT GRCh38
NC_000003.11:g.30715757_30715760delinsCATT , CM000665.1:g.30715757_30715760delinsCATT GRCh37
NC_000003.10:g.30690761_30690764delinsCATT NCBI36
NG_007490.1:g.72764_72767delinsCATT , LRG_779:g.72764_72767delinsCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1396+19_1396+22delinsCATT MANE Select ENSP00000295754.5:n.1396+19_1396+22delinsCATT
ENST00000672866.1:n.2992+19_2992+22delinsCATT
ENST00000673203.1:n.274+19_274+22delinsCATT
ENST00000295754.9:c.1396+19_1396+22delinsCATT ENSP00000295754.5:n.1396+19_1396+22delinsCATT
ENST00000359013.4:c.1471+19_1471+22delinsCATT ENSP00000351905.4:n.1471+19_1471+22delinsCATT
NM_001024847.2:c.1471+19_1471+22delinsCATT , LRG_779t1:c.1471+19_1471+22delinsCATT NP_001020018.1:n.1471+19_1471+22delinsCATT
NM_003242.5:c.1396+19_1396+22delinsCATT NP_003233.4:n.1396+19_1396+22delinsCATT
XM_011534043.1:c.1423+19_1423+22delinsCATT XP_011532345.1:n.1423+19_1423+22delinsCATT
XM_011534044.1:c.1348+19_1348+22delinsCATT XP_011532346.1:n.1348+19_1348+22delinsCATT
XM_011534045.1:c.1291+19_1291+22delinsCATT XP_011532347.1:n.1291+19_1291+22delinsCATT
XM_011534043.2:c.1423+19_1423+22delinsCATT XP_011532345.1:n.1423+19_1423+22delinsCATT
XM_011534045.3:c.1291+19_1291+22delinsCATT XP_011532347.1:n.1291+19_1291+22delinsCATT
XM_017007106.1:c.1291+19_1291+22delinsCATT XP_016862595.1:n.1291+19_1291+22delinsCATT
NM_003242.6:c.1396+19_1396+22delinsCATT MANE Select NP_003233.4:n.1396+19_1396+22delinsCATT