Canonical Allele Identifier: CA1354848182

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30617079_30617080delinsTG , CM000665.2:g.30617079_30617080delinsTG	GRCh38
NC_000003.11:g.30658571_30658572delinsTG , CM000665.1:g.30658571_30658572delinsTG	GRCh37
NC_000003.10:g.30633575_30633576delinsTG	NCBI36
NG_007490.1:g.15578_15579delinsTG , LRG_779:g.15578_15579delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10102_94+10103delinsTG MANE Select	ENSP00000295754.5:n.94+10102_94+10103delinsTG
ENST00000673250.1:n.143+2373_143+2374delinsTG
ENST00000295754.9:c.94+10102_94+10103delinsTG	ENSP00000295754.5:n.94+10102_94+10103delinsTG
ENST00000359013.4:c.95-6120_95-6119delinsTG	ENSP00000351905.4:n.95-6120_95-6119delinsTG
NM_001024847.2:c.95-6120_95-6119delinsTG , LRG_779t1:c.95-6120_95-6119delinsTG	NP_001020018.1:n.95-6120_95-6119delinsTG
NM_003242.5:c.94+10102_94+10103delinsTG	NP_003233.4:n.94+10102_94+10103delinsTG
XM_011534043.1:c.46+2373_46+2374delinsTG	XP_011532345.1:n.46+2373_46+2374delinsTG
XM_011534044.1:c.46+2373_46+2374delinsTG	XP_011532346.1:n.46+2373_46+2374delinsTG
XM_011534045.1:c.-12+10486_-12+10487delinsTG	XP_011532347.1:n.-12+10486_-12+10487delinsTG
XM_011534043.2:c.46+2373_46+2374delinsTG	XP_011532345.1:n.46+2373_46+2374delinsTG
XM_011534045.3:c.-12+10486_-12+10487delinsTG	XP_011532347.1:n.-12+10486_-12+10487delinsTG
NM_003242.6:c.94+10102_94+10103delinsTG MANE Select	NP_003233.4:n.94+10102_94+10103delinsTG