Canonical Allele Identifier: CA1354881671

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691456T= , CM000665.2:g.30691456T=	GRCh38
NC_000003.11:g.30732948T= , CM000665.1:g.30732948T=	GRCh37
NC_000003.10:g.30707952T=	NCBI36
NG_007490.1:g.89955T= , LRG_779:g.89955T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1561T= MANE Select	ENSP00000295754.5:p.Trp521=
ENST00000672050.1:n.445T=
ENST00000672866.1:n.3157T=
ENST00000673203.1:n.439T=
ENST00000295754.9:c.1561T=	ENSP00000295754.5:p.Trp521=
ENST00000359013.4:c.1636T=	ENSP00000351905.4:p.Trp546=
NM_001024847.2:c.1636T= , LRG_779t1:c.1636T=	NP_001020018.1:p.Trp546=
NM_003242.5:c.1561T=	NP_003233.4:p.Trp521=
XM_011534043.1:c.1588T=	XP_011532345.1:p.Trp530=
XM_011534044.1:c.1513T=	XP_011532346.1:p.Trp505=
XM_011534045.1:c.1456T=	XP_011532347.1:p.Trp486=
XM_011534043.2:c.1588T=	XP_011532345.1:p.Trp530=
XM_011534045.3:c.1456T=	XP_011532347.1:p.Trp486=
XM_017007106.1:c.1456T=	XP_016862595.1:p.Trp486=
NM_003242.6:c.1561T= MANE Select	NP_003233.4:p.Trp521=