Canonical Allele Identifier: CA1354874000

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674132G= , CM000665.2:g.30674132G=	GRCh38
NC_000003.11:g.30715624G= , CM000665.1:g.30715624G=	GRCh37
NC_000003.10:g.30690628G=	NCBI36
NG_007490.1:g.72631G= , LRG_779:g.72631G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1282G= MANE Select	ENSP00000295754.5:p.Glu428=
ENST00000672866.1:n.2878G=
ENST00000673203.1:n.160G=
ENST00000295754.9:c.1282G=	ENSP00000295754.5:p.Glu428=
ENST00000359013.4:c.1357G=	ENSP00000351905.4:p.Glu453=
NM_001024847.2:c.1357G= , LRG_779t1:c.1357G=	NP_001020018.1:p.Glu453=
NM_003242.5:c.1282G=	NP_003233.4:p.Glu428=
XM_011534043.1:c.1309G=	XP_011532345.1:p.Glu437=
XM_011534044.1:c.1234G=	XP_011532346.1:p.Glu412=
XM_011534045.1:c.1177G=	XP_011532347.1:p.Glu393=
XM_011534043.2:c.1309G=	XP_011532345.1:p.Glu437=
XM_011534045.3:c.1177G=	XP_011532347.1:p.Glu393=
XM_017007106.1:c.1177G=	XP_016862595.1:p.Glu393=
NM_003242.6:c.1282G= MANE Select	NP_003233.4:p.Glu428=