Canonical Allele Identifier: CA1354873189
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30672220_30672221delinsAC , CM000665.2:g.30672220_30672221delinsAC GRCh38
NC_000003.11:g.30713712_30713713delinsAC , CM000665.1:g.30713712_30713713delinsAC GRCh37
NC_000003.10:g.30688716_30688717delinsAC NCBI36
NG_007490.1:g.70719_70720delinsAC , LRG_779:g.70719_70720delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.1037_1038delinsAC MANE Select ENSP00000295754.5:p.Asp346=
ENST00000672866.1:n.2633_2634delinsAC
ENST00000295754.9:c.1037_1038delinsAC ENSP00000295754.5:p.Asp346=
ENST00000359013.4:c.1112_1113delinsAC ENSP00000351905.4:p.Asp371=
NM_001024847.2:c.1112_1113delinsAC , LRG_779t1:c.1112_1113delinsAC NP_001020018.1:p.Asp371=
NM_003242.5:c.1037_1038delinsAC NP_003233.4:p.Asp346=
XM_011534043.1:c.1064_1065delinsAC XP_011532345.1:p.Asp355=
XM_011534044.1:c.989_990delinsAC XP_011532346.1:p.Asp330=
XM_011534045.1:c.932_933delinsAC XP_011532347.1:p.Asp311=
XM_011534043.2:c.1064_1065delinsAC XP_011532345.1:p.Asp355=
XM_011534045.3:c.932_933delinsAC XP_011532347.1:p.Asp311=
XM_017007106.1:c.932_933delinsAC XP_016862595.1:p.Asp311=
NM_003242.6:c.1037_1038delinsAC MANE Select NP_003233.4:p.Asp346=