Canonical Allele Identifier: CA1354848152

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30616992_30616994delinsCTG , CM000665.2:g.30616992_30616994delinsCTG	GRCh38
NC_000003.11:g.30658484_30658486delinsCTG , CM000665.1:g.30658484_30658486delinsCTG	GRCh37
NC_000003.10:g.30633488_30633490delinsCTG	NCBI36
NG_007490.1:g.15491_15493delinsCTG , LRG_779:g.15491_15493delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10015_94+10017delinsCTG MANE Select	ENSP00000295754.5:n.94+10015_94+10017delinsCTG
ENST00000673250.1:n.143+2286_143+2288delinsCTG
ENST00000295754.9:c.94+10015_94+10017delinsCTG	ENSP00000295754.5:n.94+10015_94+10017delinsCTG
ENST00000359013.4:c.95-6207_95-6205delinsCTG	ENSP00000351905.4:n.95-6207_95-6205delinsCTG
NM_001024847.2:c.95-6207_95-6205delinsCTG , LRG_779t1:c.95-6207_95-6205delinsCTG	NP_001020018.1:n.95-6207_95-6205delinsCTG
NM_003242.5:c.94+10015_94+10017delinsCTG	NP_003233.4:n.94+10015_94+10017delinsCTG
XM_011534043.1:c.46+2286_46+2288delinsCTG	XP_011532345.1:n.46+2286_46+2288delinsCTG
XM_011534044.1:c.46+2286_46+2288delinsCTG	XP_011532346.1:n.46+2286_46+2288delinsCTG
XM_011534045.1:c.-12+10399_-12+10401delinsCTG	XP_011532347.1:n.-12+10399_-12+10401delinsCTG
XM_011534043.2:c.46+2286_46+2288delinsCTG	XP_011532345.1:n.46+2286_46+2288delinsCTG
XM_011534045.3:c.-12+10399_-12+10401delinsCTG	XP_011532347.1:n.-12+10399_-12+10401delinsCTG
NM_003242.6:c.94+10015_94+10017delinsCTG MANE Select	NP_003233.4:n.94+10015_94+10017delinsCTG