Canonical Allele Identifier: CA1354863228

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30649608_30649609delinsTG , CM000665.2:g.30649608_30649609delinsTG	GRCh38
NC_000003.11:g.30691100_30691101delinsTG , CM000665.1:g.30691100_30691101delinsTG	GRCh37
NC_000003.10:g.30666104_30666105delinsTG	NCBI36
NG_007490.1:g.48107_48108delinsTG , LRG_779:g.48107_48108delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.264-662_264-661delinsTG MANE Select	ENSP00000295754.5:n.264-662_264-661delinsTG
ENST00000672866.1:n.1860-662_1860-661delinsTG
ENST00000673250.1:n.388-662_388-661delinsTG
ENST00000295754.9:c.264-662_264-661delinsTG	ENSP00000295754.5:n.264-662_264-661delinsTG
ENST00000359013.4:c.339-662_339-661delinsTG	ENSP00000351905.4:n.339-662_339-661delinsTG
NM_001024847.2:c.339-662_339-661delinsTG , LRG_779t1:c.339-662_339-661delinsTG	NP_001020018.1:n.339-662_339-661delinsTG
NM_003242.5:c.264-662_264-661delinsTG	NP_003233.4:n.264-662_264-661delinsTG
XM_011534043.1:c.291-662_291-661delinsTG	XP_011532345.1:n.291-662_291-661delinsTG
XM_011534044.1:c.216-662_216-661delinsTG	XP_011532346.1:n.216-662_216-661delinsTG
XM_011534045.1:c.159-662_159-661delinsTG	XP_011532347.1:n.159-662_159-661delinsTG
XM_011534043.2:c.291-662_291-661delinsTG	XP_011532345.1:n.291-662_291-661delinsTG
XM_011534045.3:c.159-662_159-661delinsTG	XP_011532347.1:n.159-662_159-661delinsTG
XM_017007106.1:c.159-662_159-661delinsTG	XP_016862595.1:n.159-662_159-661delinsTG
NM_003242.6:c.264-662_264-661delinsTG MANE Select	NP_003233.4:n.264-662_264-661delinsTG