Canonical Allele Identifier: CA1354873986

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30674113T= , CM000665.2:g.30674113T=	GRCh38
NC_000003.11:g.30715605T= , CM000665.1:g.30715605T=	GRCh37
NC_000003.10:g.30690609T=	NCBI36
NG_007490.1:g.72612T= , LRG_779:g.72612T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1263T= MANE Select	ENSP00000295754.5:p.Thr421=
ENST00000672866.1:n.2859T=
ENST00000673203.1:n.141T=
ENST00000295754.9:c.1263T=	ENSP00000295754.5:p.Thr421=
ENST00000359013.4:c.1338T=	ENSP00000351905.4:p.Thr446=
NM_001024847.2:c.1338T= , LRG_779t1:c.1338T=	NP_001020018.1:p.Thr446=
NM_003242.5:c.1263T=	NP_003233.4:p.Thr421=
XM_011534043.1:c.1290T=	XP_011532345.1:p.Thr430=
XM_011534044.1:c.1215T=	XP_011532346.1:p.Thr405=
XM_011534045.1:c.1158T=	XP_011532347.1:p.Thr386=
XM_011534043.2:c.1290T=	XP_011532345.1:p.Thr430=
XM_011534045.3:c.1158T=	XP_011532347.1:p.Thr386=
XM_017007106.1:c.1158T=	XP_016862595.1:p.Thr386=
NM_003242.6:c.1263T= MANE Select	NP_003233.4:p.Thr421=