Canonical Allele Identifier: CA1354873997

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674129C= , CM000665.2:g.30674129C=	GRCh38
NC_000003.11:g.30715621C= , CM000665.1:g.30715621C=	GRCh37
NC_000003.10:g.30690625C=	NCBI36
NG_007490.1:g.72628C= , LRG_779:g.72628C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1279C= MANE Select	ENSP00000295754.5:p.Pro427=
ENST00000672866.1:n.2875C=
ENST00000673203.1:n.157C=
ENST00000295754.9:c.1279C=	ENSP00000295754.5:p.Pro427=
ENST00000359013.4:c.1354C=	ENSP00000351905.4:p.Pro452=
NM_001024847.2:c.1354C= , LRG_779t1:c.1354C=	NP_001020018.1:p.Pro452=
NM_003242.5:c.1279C=	NP_003233.4:p.Pro427=
XM_011534043.1:c.1306C=	XP_011532345.1:p.Pro436=
XM_011534044.1:c.1231C=	XP_011532346.1:p.Pro411=
XM_011534045.1:c.1174C=	XP_011532347.1:p.Pro392=
XM_011534043.2:c.1306C=	XP_011532345.1:p.Pro436=
XM_011534045.3:c.1174C=	XP_011532347.1:p.Pro392=
XM_017007106.1:c.1174C=	XP_016862595.1:p.Pro392=
NM_003242.6:c.1279C= MANE Select	NP_003233.4:p.Pro427=