Canonical Allele Identifier: CA1354874004

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674143A= , CM000665.2:g.30674143A=	GRCh38
NC_000003.11:g.30715635A= , CM000665.1:g.30715635A=	GRCh37
NC_000003.10:g.30690639A=	NCBI36
NG_007490.1:g.72642A= , LRG_779:g.72642A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1293A= MANE Select	ENSP00000295754.5:p.Glu431=
ENST00000672866.1:n.2889A=
ENST00000673203.1:n.171A=
ENST00000295754.9:c.1293A=	ENSP00000295754.5:p.Glu431=
ENST00000359013.4:c.1368A=	ENSP00000351905.4:p.Glu456=
NM_001024847.2:c.1368A= , LRG_779t1:c.1368A=	NP_001020018.1:p.Glu456=
NM_003242.5:c.1293A=	NP_003233.4:p.Glu431=
XM_011534043.1:c.1320A=	XP_011532345.1:p.Glu440=
XM_011534044.1:c.1245A=	XP_011532346.1:p.Glu415=
XM_011534045.1:c.1188A=	XP_011532347.1:p.Glu396=
XM_011534043.2:c.1320A=	XP_011532345.1:p.Glu440=
XM_011534045.3:c.1188A=	XP_011532347.1:p.Glu396=
XM_017007106.1:c.1188A=	XP_016862595.1:p.Glu396=
NM_003242.6:c.1293A= MANE Select	NP_003233.4:p.Glu431=