Canonical Allele Identifier: CA2755703655

Gene: TGFBR2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.30617091_30617094dup , CM000665.2:g.30617091_30617094dup	GRCh38
NC_000003.11:g.30658583_30658586dup , CM000665.1:g.30658583_30658586dup	GRCh37
NC_000003.10:g.30633587_30633590dup	NCBI36
NG_007490.1:g.15590_15593dup , LRG_779:g.15590_15593dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295754.10:c.94+10114_94+10117dup MANE Select	ENSP00000295754.5:n.94+10114_94+10117dup
ENST00000673250.1:n.143+2385_143+2388dup
ENST00000295754.9:c.94+10114_94+10117dup	ENSP00000295754.5:n.94+10114_94+10117dup
ENST00000359013.4:c.95-6108_95-6105dup	ENSP00000351905.4:n.95-6108_95-6105dup
NM_001024847.2:c.95-6108_95-6105dup , LRG_779t1:c.95-6108_95-6105dup	NP_001020018.1:n.95-6108_95-6105dup
NM_003242.5:c.94+10114_94+10117dup	NP_003233.4:n.94+10114_94+10117dup
XM_011534043.1:c.46+2385_46+2388dup	XP_011532345.1:n.46+2385_46+2388dup
XM_011534044.1:c.46+2385_46+2388dup	XP_011532346.1:n.46+2385_46+2388dup
XM_011534045.1:c.-12+10498_-12+10501dup	XP_011532347.1:n.-12+10498_-12+10501dup
XM_011534043.2:c.46+2385_46+2388dup	XP_011532345.1:n.46+2385_46+2388dup
XM_011534045.3:c.-12+10498_-12+10501dup	XP_011532347.1:n.-12+10498_-12+10501dup
NM_003242.6:c.94+10114_94+10117dup MANE Select	NP_003233.4:n.94+10114_94+10117dup