Canonical Allele Identifier: CA2831039748

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30691498_30691504delinsA , CM000665.2:g.30691498_30691504delinsA	GRCh38
NC_000003.11:g.30732990_30732996delinsA , CM000665.1:g.30732990_30732996delinsA	GRCh37
NC_000003.10:g.30707994_30708000delinsA	NCBI36
NG_007490.1:g.89997_90003delinsA , LRG_779:g.89997_90003delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.1603_1609delinsA MANE Select	ENSP00000295754.5:p.Ala535_Arg537delinsSer
ENST00000672050.1:n.487_493delinsA
ENST00000672866.1:n.3199_3205delinsA
ENST00000673203.1:n.481_487delinsA
ENST00000295754.9:c.1603_1609delinsA	ENSP00000295754.5:p.Ala535_Arg537delinsSer
ENST00000359013.4:c.1678_1684delinsA	ENSP00000351905.4:p.Ala560_Arg562delinsSer
NM_001024847.2:c.1678_1684delinsA , LRG_779t1:c.1678_1684delinsA	NP_001020018.1:p.Ala560_Arg562delinsSer
NM_003242.5:c.1603_1609delinsA	NP_003233.4:p.Ala535_Arg537delinsSer
XM_011534043.1:c.1630_1636delinsA	XP_011532345.1:p.Ala544_Arg546delinsSer
XM_011534044.1:c.1555_1561delinsA	XP_011532346.1:p.Ala519_Arg521delinsSer
XM_011534045.1:c.1498_1504delinsA	XP_011532347.1:p.Ala500_Arg502delinsSer
XM_011534043.2:c.1630_1636delinsA	XP_011532345.1:p.Ala544_Arg546delinsSer
XM_011534045.3:c.1498_1504delinsA	XP_011532347.1:p.Ala500_Arg502delinsSer
XM_017007106.1:c.1498_1504delinsA	XP_016862595.1:p.Ala500_Arg502delinsSer
NM_003242.6:c.1603_1609delinsA MANE Select	NP_003233.4:p.Ala535_Arg537delinsSer