Canonical Allele Identifier: CA963264511
Gene: BMP4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.53950804_53950805insAGAGCCGAAGCTCTGCAGAGGAGATCG , CM000676.2:g.53950804_53950805insAGAGCCGAAGCTCTGCAGAGGAGATCG GRCh38
NC_000014.8:g.54417522_54417523insAGAGCCGAAGCTCTGCAGAGGAGATCG , CM000676.1:g.54417522_54417523insAGAGCCGAAGCTCTGCAGAGGAGATCG GRCh37
NC_000014.7:g.53487272_53487273insAGAGCCGAAGCTCTGCAGAGGAGATCG NCBI36
NG_009215.1:g.11032_11033insCGATCTCCTCTGCAGAGCTTCGGCTCT

Transcript Alleles

HGVS Amino-acid change
ENST00000245451.9:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT MANE Select ENSP00000245451.4:p.Val152delinsAlaIleSer...
ENST00000245451.8:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT ENSP00000245451.4:p.Val152delinsAlaIleSer...
ENST00000417573.5:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT ENSP00000394165.1:p.Val152delinsAlaIleSer...
ENST00000558961.1:c.312_313insCGATCTCCTCTGCAGAGCTTCGGCTCT ENSP00000453691.1:p.Arg104_Ter105insArgSe...
ENST00000558984.1:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT ENSP00000454134.1:p.Val152delinsAlaIleSer...
ENST00000559087.5:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT ENSP00000453485.1:p.Val152delinsAlaIleSer...
ENST00000559501.1:c.265_266insCGATCTCCTCTGCAGAGCTTCGGCTCT ENSP00000453365.1:p.Val89delinsAlaIleSerS...
NM_001202.3:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001193.2:p.Val152delinsAlaIleSerSerAla...
NM_130850.2:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_570911.2:p.Val152delinsAlaIleSerSerAla...
NM_130851.2:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_570912.2:p.Val152delinsAlaIleSerSerAla...
XM_005268015.3:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT XP_005268072.1:p.Val152delinsAlaIleSerSer...
NM_001202.5:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001193.2:p.Val152delinsAlaIleSerSerAla...
NM_001347912.1:c.595_596insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334841.1:p.Val199delinsAlaIleSerSer...
NM_001347913.1:c.265_266insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334842.1:p.Val89delinsAlaIleSerSerA...
NM_001347914.1:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334843.1:p.Val152delinsAlaIleSerSer...
NM_001347915.1:c.265_266insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334844.1:p.Val89delinsAlaIleSerSerA...
NM_001347916.1:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334845.1:p.Val152delinsAlaIleSerSer...
NM_001347917.1:c.265_266insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334846.1:p.Val89delinsAlaIleSerSerA...
NM_130850.4:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_570911.2:p.Val152delinsAlaIleSerSerAla...
NM_130851.3:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_570912.2:p.Val152delinsAlaIleSerSerAla...
NM_001202.6:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT MANE Select NP_001193.2:p.Val152delinsAlaIleSerSerAla...
NM_130850.5:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_570911.2:p.Val152delinsAlaIleSerSerAla...
NM_001347913.2:c.265_266insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334842.1:p.Val89delinsAlaIleSerSerA...
NM_001347914.2:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334843.1:p.Val152delinsAlaIleSerSer...
NM_001347915.2:c.265_266insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_001334844.1:p.Val89delinsAlaIleSerSerA...
NM_130851.4:c.454_455insCGATCTCCTCTGCAGAGCTTCGGCTCT NP_570912.2:p.Val152delinsAlaIleSerSerAla...