Canonical Allele Identifier: CA2573134353
Gene: BMPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1443330
ClinVar RCV Id: RCV001987486
dbSNP Id: rs2105962353

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.202467617del , CM000664.2:g.202467617del GRCh38
NC_000002.11:g.203332340del , CM000664.1:g.203332340del GRCh37
NC_000002.10:g.203040585del NCBI36
NG_009363.1:g.96291del , LRG_712:g.96291del

Transcript Alleles

HGVS Amino-acid change
ENST00000374580.10:c.346del MANE Select ENSP00000363708.4:p.Cys116AlafsTer?
ENST00000638587.1:c.277del ENSP00000491062.1:p.Cys93AlafsTer?
ENST00000374574.2:c.346del ENSP00000363702.2:p.Cys116AlafsTer?
ENST00000374580.8:c.346del ENSP00000363708.4:p.Cys116AlafsTer?
ENST00000479069.1:n.253del
NM_001204.6:c.346del , LRG_712t1:c.346del NP_001195.2:p.Cys116AlafsTer?
XM_011511687.1:c.346del XP_011509989.1:p.Cys116AlafsTer?
XM_011511688.1:c.346del XP_011509990.1:p.Cys116AlafsTer?
NM_001204.7:c.346del MANE Select NP_001195.2:p.Cys116AlafsTer?