Canonical Allele Identifier: CA658797466
Gene: BMPR1A HGNC NCBI

Linked Data

ClinVar Variation Id: 529921
ClinVar RCV Id: RCV002234491
dbSNP Id: rs1554890759

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86917189dup , CM000672.2:g.86917189dup GRCh38
NC_000010.10:g.88676946dup , CM000672.1:g.88676946dup GRCh37
NC_000010.9:g.88666926dup NCBI36
NG_009362.1:g.165551dup , LRG_298:g.165551dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.731dup ENSP00000483569.2:p.Tyr245IlefsTer23
ENST00000635816.2:c.731dup ENSP00000489707.1:p.Tyr245IlefsTer23
ENST00000636056.2:c.731dup ENSP00000490273.1:p.Tyr245IlefsTer23
ENST00000372037.8:c.731dup MANE Select ENSP00000361107.2:p.Tyr245IlefsTer23
ENST00000635816.1:c.731dup ENSP00000489707.1:p.Tyr245IlefsTer23
ENST00000636056.1:c.731dup ENSP00000490273.1:p.Tyr245IlefsTer23
ENST00000638429.1:c.731dup ENSP00000492290.1:p.Tyr245IlefsTer23
ENST00000372037.7:c.731dup ENSP00000361107.1:p.Tyr245IlefsTer23
NM_004329.2:c.731dup , LRG_298t1:c.731dup NP_004320.2:p.Tyr245IlefsTer23
XM_011540103.1:c.731dup XP_011538405.1:p.Tyr245IlefsTer23
XM_011540104.1:c.731dup XP_011538406.1:p.Tyr245IlefsTer23
XM_011540103.2:c.731dup XP_011538405.1:p.Tyr245IlefsTer23
XM_011540104.2:c.731dup XP_011538406.1:p.Tyr245IlefsTer23
NM_004329.3:c.731dup MANE Select NP_004320.2:p.Tyr245IlefsTer23