Canonical Allele Identifier: CA2702374037

Gene: TGFBR2

Linked Data

• dbSNP Id: rs2125439562

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674278_30674279insGCA , CM000665.2:g.30674278_30674279insGCA	GRCh38
NC_000003.11:g.30715770_30715771insGCA , CM000665.1:g.30715770_30715771insGCA	GRCh37
NC_000003.10:g.30690774_30690775insGCA	NCBI36
NG_007490.1:g.72777_72778insGCA , LRG_779:g.72777_72778insGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1396+32_1396+33insGCA MANE Select	ENSP00000295754.5:n.1396+32_1396+33insGCA
ENST00000672866.1:n.2992+32_2992+33insGCA
ENST00000673203.1:n.274+32_274+33insGCA
ENST00000295754.9:c.1396+32_1396+33insGCA	ENSP00000295754.5:n.1396+32_1396+33insGCA
ENST00000359013.4:c.1471+32_1471+33insGCA	ENSP00000351905.4:n.1471+32_1471+33insGCA
NM_001024847.2:c.1471+32_1471+33insGCA , LRG_779t1:c.1471+32_1471+33insGCA	NP_001020018.1:n.1471+32_1471+33insGCA
NM_003242.5:c.1396+32_1396+33insGCA	NP_003233.4:n.1396+32_1396+33insGCA
XM_011534043.1:c.1423+32_1423+33insGCA	XP_011532345.1:n.1423+32_1423+33insGCA
XM_011534044.1:c.1348+32_1348+33insGCA	XP_011532346.1:n.1348+32_1348+33insGCA
XM_011534045.1:c.1291+32_1291+33insGCA	XP_011532347.1:n.1291+32_1291+33insGCA
XM_011534043.2:c.1423+32_1423+33insGCA	XP_011532345.1:n.1423+32_1423+33insGCA
XM_011534045.3:c.1291+32_1291+33insGCA	XP_011532347.1:n.1291+32_1291+33insGCA
XM_017007106.1:c.1291+32_1291+33insGCA	XP_016862595.1:n.1291+32_1291+33insGCA
NM_003242.6:c.1396+32_1396+33insGCA MANE Select	NP_003233.4:n.1396+32_1396+33insGCA