Canonical Allele Identifier: CA322561

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691459G>A , CM000665.2:g.30691459G>A	GRCh38
NC_000003.11:g.30732951G>A , CM000665.1:g.30732951G>A	GRCh37
NC_000003.10:g.30707955G>A	NCBI36
NG_007490.1:g.89958G>A , LRG_779:g.89958G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003242.6:c.1564G>A MANE Select	NP_003233.4:p.Asp522Asn
ENST00000295754.10:c.1564G>A MANE Select	ENSP00000295754.5:p.Asp522Asn
NM_001024847.2:c.1639G>A , LRG_779t1:c.1639G>A	NP_001020018.1:p.Asp547Asn
NM_003242.5:c.1564G>A	NP_003233.4:p.Asp522Asn
ENST00000295754.9:c.1564G>A	ENSP00000295754.5:p.Asp522Asn
ENST00000359013.4:c.1639G>A	ENSP00000351905.4:p.Asp547Asn
ENST00000672050.1:n.448G>A
ENST00000672866.1:n.3160G>A
ENST00000673203.1:n.442G>A
XM_011534043.1:c.1591G>A	XP_011532345.1:p.Asp531Asn
XM_011534043.2:c.1591G>A	XP_011532345.1:p.Asp531Asn
XM_011534044.1:c.1516G>A	XP_011532346.1:p.Asp506Asn
XM_011534045.1:c.1459G>A	XP_011532347.1:p.Asp487Asn
XM_011534045.3:c.1459G>A	XP_011532347.1:p.Asp487Asn
XM_017007106.1:c.1459G>A	XP_016862595.1:p.Asp487Asn