Canonical Allele Identifier: CA1354871657
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30668762_30668763delinsCA , CM000665.2:g.30668762_30668763delinsCA GRCh38
NC_000003.11:g.30710254_30710255delinsCA , CM000665.1:g.30710254_30710255delinsCA GRCh37
NC_000003.10:g.30685258_30685259delinsCA NCBI36
NG_007490.1:g.67261_67262delinsCA , LRG_779:g.67261_67262delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.455-2876_455-2875delinsCA MANE Select ENSP00000295754.5:n.455-2876_455-2875delinsCA
ENST00000672866.1:n.2051-2876_2051-2875delinsCA
ENST00000295754.9:c.455-2876_455-2875delinsCA ENSP00000295754.5:n.455-2876_455-2875delinsCA
ENST00000359013.4:c.530-2876_530-2875delinsCA ENSP00000351905.4:n.530-2876_530-2875delinsCA
NM_001024847.2:c.530-2876_530-2875delinsCA , LRG_779t1:c.530-2876_530-2875delinsCA NP_001020018.1:n.530-2876_530-2875delinsCA
NM_003242.5:c.455-2876_455-2875delinsCA NP_003233.4:n.455-2876_455-2875delinsCA
XM_011534043.1:c.482-2876_482-2875delinsCA XP_011532345.1:n.482-2876_482-2875delinsCA
XM_011534044.1:c.407-2876_407-2875delinsCA XP_011532346.1:n.407-2876_407-2875delinsCA
XM_011534045.1:c.350-2876_350-2875delinsCA XP_011532347.1:n.350-2876_350-2875delinsCA
XM_011534043.2:c.482-2876_482-2875delinsCA XP_011532345.1:n.482-2876_482-2875delinsCA
XM_011534045.3:c.350-2876_350-2875delinsCA XP_011532347.1:n.350-2876_350-2875delinsCA
XM_017007106.1:c.350-2876_350-2875delinsCA XP_016862595.1:n.350-2876_350-2875delinsCA
NM_003242.6:c.455-2876_455-2875delinsCA MANE Select NP_003233.4:n.455-2876_455-2875delinsCA