Canonical Allele Identifier: CA1354844277
Gene: TGFBR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.30608489_30608492delinsAGAG , CM000665.2:g.30608489_30608492delinsAGAG GRCh38
NC_000003.11:g.30649981_30649984delinsAGAG , CM000665.1:g.30649981_30649984delinsAGAG GRCh37
NC_000003.10:g.30624985_30624988delinsAGAG NCBI36
NG_007490.1:g.6988_6991delinsAGAG , LRG_779:g.6988_6991delinsAGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000295754.10:c.94+1512_94+1515delinsAGAG MANE Select ENSP00000295754.5:n.94+1512_94+1515delinsAGAG
ENST00000295754.9:c.94+1512_94+1515delinsAGAG ENSP00000295754.5:n.94+1512_94+1515delinsAGAG
ENST00000359013.4:c.94+1512_94+1515delinsAGAG ENSP00000351905.4:n.94+1512_94+1515delinsAGAG
NM_001024847.2:c.94+1512_94+1515delinsAGAG , LRG_779t1:c.94+1512_94+1515delinsAGAG NP_001020018.1:n.94+1512_94+1515delinsAGAG
NM_003242.5:c.94+1512_94+1515delinsAGAG NP_003233.4:n.94+1512_94+1515delinsAGAG
XM_011534045.1:c.-12+1896_-12+1899delinsAGAG XP_011532347.1:n.-12+1896_-12+1899delinsAGAG
XM_011534045.3:c.-12+1896_-12+1899delinsAGAG XP_011532347.1:n.-12+1896_-12+1899delinsAGAG
NM_003242.6:c.94+1512_94+1515delinsAGAG MANE Select NP_003233.4:n.94+1512_94+1515delinsAGAG