Canonical Allele Identifier: CA1354874002

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674137C= , CM000665.2:g.30674137C=	GRCh38
NC_000003.11:g.30715629C= , CM000665.1:g.30715629C=	GRCh37
NC_000003.10:g.30690633C=	NCBI36
NG_007490.1:g.72636C= , LRG_779:g.72636C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.1287C= MANE Select	ENSP00000295754.5:p.Val429=
ENST00000672866.1:n.2883C=
ENST00000673203.1:n.165C=
ENST00000295754.9:c.1287C=	ENSP00000295754.5:p.Val429=
ENST00000359013.4:c.1362C=	ENSP00000351905.4:p.Val454=
NM_001024847.2:c.1362C= , LRG_779t1:c.1362C=	NP_001020018.1:p.Val454=
NM_003242.5:c.1287C=	NP_003233.4:p.Val429=
XM_011534043.1:c.1314C=	XP_011532345.1:p.Val438=
XM_011534044.1:c.1239C=	XP_011532346.1:p.Val413=
XM_011534045.1:c.1182C=	XP_011532347.1:p.Val394=
XM_011534043.2:c.1314C=	XP_011532345.1:p.Val438=
XM_011534045.3:c.1182C=	XP_011532347.1:p.Val394=
XM_017007106.1:c.1182C=	XP_016862595.1:p.Val394=
NM_003242.6:c.1287C= MANE Select	NP_003233.4:p.Val429=