Canonical Allele Identifier: CA2568359516

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30608612_30608613insCC , CM000665.2:g.30608612_30608613insCC	GRCh38
NC_000003.11:g.30650104_30650105insCC , CM000665.1:g.30650104_30650105insCC	GRCh37
NC_000003.10:g.30625108_30625109insCC	NCBI36
NG_007490.1:g.7111_7112insCC , LRG_779:g.7111_7112insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+1635_94+1636insCC MANE Select	ENSP00000295754.5:n.94+1635_94+1636insCC
ENST00000295754.9:c.94+1635_94+1636insCC	ENSP00000295754.5:n.94+1635_94+1636insCC
ENST00000359013.4:c.94+1635_94+1636insCC	ENSP00000351905.4:n.94+1635_94+1636insCC
NM_001024847.2:c.94+1635_94+1636insCC , LRG_779t1:c.94+1635_94+1636insCC	NP_001020018.1:n.94+1635_94+1636insCC
NM_003242.5:c.94+1635_94+1636insCC	NP_003233.4:n.94+1635_94+1636insCC
XM_011534045.1:c.-12+2019_-12+2020insCC	XP_011532347.1:n.-12+2019_-12+2020insCC
XM_011534045.3:c.-12+2019_-12+2020insCC	XP_011532347.1:n.-12+2019_-12+2020insCC
NM_003242.6:c.94+1635_94+1636insCC MANE Select	NP_003233.4:n.94+1635_94+1636insCC