Canonical Allele Identifier: CA915941645
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 812815
ClinVar RCV Id: RCV001003688
dbSNP Id: rs1574488357

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202518891del , CM000664.2:g.202518891del GRCh38
NC_000002.11:g.203383614del , CM000664.1:g.203383614del GRCh37
NC_000002.10:g.203091859del NCBI36
NG_009363.1:g.147565del , LRG_712:g.147565del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.691del MANE Select ENSP00000363708.4:p.Val231CysfsTer21
ENST00000638587.1:c.622del ENSP00000491062.1:p.Val208CysfsTer21
ENST00000374574.2:c.691del ENSP00000363702.2:p.Val231CysfsTer21
ENST00000374580.8:c.691del ENSP00000363708.4:p.Val231CysfsTer21
NM_001204.6:c.691del , LRG_712t1:c.691del NP_001195.2:p.Val231CysfsTer21
XM_011511687.1:c.691del XP_011509989.1:p.Val231CysfsTer21
XM_011511688.1:c.691del XP_011509990.1:p.Val231CysfsTer21
NM_001204.7:c.691del MANE Select NP_001195.2:p.Val231CysfsTer21