Canonical Allele Identifier: CA1354871663
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30668774_30668775delinsAT , CM000665.2:g.30668774_30668775delinsAT GRCh38
NC_000003.11:g.30710266_30710267delinsAT , CM000665.1:g.30710266_30710267delinsAT GRCh37
NC_000003.10:g.30685270_30685271delinsAT NCBI36
NG_007490.1:g.67273_67274delinsAT , LRG_779:g.67273_67274delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.455-2864_455-2863delinsAT MANE Select ENSP00000295754.5:n.455-2864_455-2863delinsAT
ENST00000672866.1:n.2051-2864_2051-2863delinsAT
ENST00000295754.9:c.455-2864_455-2863delinsAT ENSP00000295754.5:n.455-2864_455-2863delinsAT
ENST00000359013.4:c.530-2864_530-2863delinsAT ENSP00000351905.4:n.530-2864_530-2863delinsAT
NM_001024847.2:c.530-2864_530-2863delinsAT , LRG_779t1:c.530-2864_530-2863delinsAT NP_001020018.1:n.530-2864_530-2863delinsAT
NM_003242.5:c.455-2864_455-2863delinsAT NP_003233.4:n.455-2864_455-2863delinsAT
XM_011534043.1:c.482-2864_482-2863delinsAT XP_011532345.1:n.482-2864_482-2863delinsAT
XM_011534044.1:c.407-2864_407-2863delinsAT XP_011532346.1:n.407-2864_407-2863delinsAT
XM_011534045.1:c.350-2864_350-2863delinsAT XP_011532347.1:n.350-2864_350-2863delinsAT
XM_011534043.2:c.482-2864_482-2863delinsAT XP_011532345.1:n.482-2864_482-2863delinsAT
XM_011534045.3:c.350-2864_350-2863delinsAT XP_011532347.1:n.350-2864_350-2863delinsAT
XM_017007106.1:c.350-2864_350-2863delinsAT XP_016862595.1:n.350-2864_350-2863delinsAT
NM_003242.6:c.455-2864_455-2863delinsAT MANE Select NP_003233.4:n.455-2864_455-2863delinsAT