Canonical Allele Identifier: CA325169

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30650460G>A , CM000665.2:g.30650460G>A	GRCh38
NC_000003.11:g.30691952G>A , CM000665.1:g.30691952G>A	GRCh37
NC_000003.10:g.30666956G>A	NCBI36
NG_007490.1:g.48959G>A , LRG_779:g.48959G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.454G>A MANE Select	ENSP00000295754.5:p.Glu152Lys
ENST00000672866.1:n.2050G>A
ENST00000295754.9:c.454G>A	ENSP00000295754.5:p.Glu152Lys
ENST00000359013.4:c.529G>A	ENSP00000351905.4:p.Glu177Lys
NM_001024847.2:c.529G>A , LRG_779t1:c.529G>A	NP_001020018.1:p.Glu177Lys
NM_003242.5:c.454G>A	NP_003233.4:p.Glu152Lys
XM_011534043.1:c.481G>A	XP_011532345.1:p.Glu161Lys
XM_011534044.1:c.406G>A	XP_011532346.1:p.Glu136Lys
XM_011534045.1:c.349G>A	XP_011532347.1:p.Glu117Lys
XM_011534043.2:c.481G>A	XP_011532345.1:p.Glu161Lys
XM_011534045.3:c.349G>A	XP_011532347.1:p.Glu117Lys
XM_017007106.1:c.349G>A	XP_016862595.1:p.Glu117Lys
NM_003242.6:c.454G>A MANE Select	NP_003233.4:p.Glu152Lys