Canonical Allele Identifier: CA351809591

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691471G>A , CM000665.2:g.30691471G>A	GRCh38
NC_000003.11:g.30732963G>A , CM000665.1:g.30732963G>A	GRCh37
NC_000003.10:g.30707967G>A	NCBI36
NG_007490.1:g.89970G>A , LRG_779:g.89970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1576G>A MANE Select	ENSP00000295754.5:p.Glu526Lys
ENST00000672050.1:n.460G>A
ENST00000672866.1:n.3172G>A
ENST00000673203.1:n.454G>A
ENST00000295754.9:c.1576G>A	ENSP00000295754.5:p.Glu526Lys
ENST00000359013.4:c.1651G>A	ENSP00000351905.4:p.Glu551Lys
NM_001024847.2:c.1651G>A , LRG_779t1:c.1651G>A	NP_001020018.1:p.Glu551Lys
NM_003242.5:c.1576G>A	NP_003233.4:p.Glu526Lys
XM_011534043.1:c.1603G>A	XP_011532345.1:p.Glu535Lys
XM_011534044.1:c.1528G>A	XP_011532346.1:p.Glu510Lys
XM_011534045.1:c.1471G>A	XP_011532347.1:p.Glu491Lys
XM_011534043.2:c.1603G>A	XP_011532345.1:p.Glu535Lys
XM_011534045.3:c.1471G>A	XP_011532347.1:p.Glu491Lys
XM_017007106.1:c.1471G>A	XP_016862595.1:p.Glu491Lys
NM_003242.6:c.1576G>A MANE Select	NP_003233.4:p.Glu526Lys