Canonical Allele Identifier: CA1354844290

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30608538_30608539delinsAG , CM000665.2:g.30608538_30608539delinsAG	GRCh38
NC_000003.11:g.30650030_30650031delinsAG , CM000665.1:g.30650030_30650031delinsAG	GRCh37
NC_000003.10:g.30625034_30625035delinsAG	NCBI36
NG_007490.1:g.7037_7038delinsAG , LRG_779:g.7037_7038delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000295754.10:c.94+1561_94+1562delinsAG MANE Select	ENSP00000295754.5:n.94+1561_94+1562delinsAG
ENST00000295754.9:c.94+1561_94+1562delinsAG	ENSP00000295754.5:n.94+1561_94+1562delinsAG
ENST00000359013.4:c.94+1561_94+1562delinsAG	ENSP00000351905.4:n.94+1561_94+1562delinsAG
NM_001024847.2:c.94+1561_94+1562delinsAG , LRG_779t1:c.94+1561_94+1562delinsAG	NP_001020018.1:n.94+1561_94+1562delinsAG
NM_003242.5:c.94+1561_94+1562delinsAG	NP_003233.4:n.94+1561_94+1562delinsAG
XM_011534045.1:c.-12+1945_-12+1946delinsAG	XP_011532347.1:n.-12+1945_-12+1946delinsAG
XM_011534045.3:c.-12+1945_-12+1946delinsAG	XP_011532347.1:n.-12+1945_-12+1946delinsAG
NM_003242.6:c.94+1561_94+1562delinsAG MANE Select	NP_003233.4:n.94+1561_94+1562delinsAG