Canonical Allele Identifier: CA10578878

Gene: BMPR1A

Linked Data

• ClinVar Variation Id: 233491
• ClinVar RCV Id: RCV000214964 ; RCV002229316
• dbSNP Id: rs876660442
• MyVariant Identifiers: chr10:g.88659622dupA (hg19) ; chr10:g.86899865dupA (hg38)
• PubMed: PMID:16436638

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86899865dup , CM000672.2:g.86899865dup	GRCh38
NC_000010.10:g.88659622dup , CM000672.1:g.88659622dup	GRCh37
NC_000010.9:g.88649602dup	NCBI36
NG_009362.1:g.148227dup , LRG_298:g.148227dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.405dup	ENSP00000483569.2:p.Pro136ThrfsTer13
ENST00000635816.2:c.405dup	ENSP00000489707.1:p.Pro136ThrfsTer13
ENST00000636056.2:c.405dup	ENSP00000490273.1:p.Pro136ThrfsTer13
ENST00000372037.8:c.405dup MANE Select	ENSP00000361107.2:p.Pro136ThrfsTer13
ENST00000635816.1:c.405dup	ENSP00000489707.1:p.Pro136ThrfsTer13
ENST00000636056.1:c.405dup	ENSP00000490273.1:p.Pro136ThrfsTer13
ENST00000638429.1:c.405dup	ENSP00000492290.1:p.Pro136ThrfsTer13
ENST00000372037.7:c.405dup	ENSP00000361107.1:p.Pro136ThrfsTer13
NM_004329.2:c.405dup , LRG_298t1:c.405dup	NP_004320.2:p.Pro136ThrfsTer13
XM_011540103.1:c.405dup	XP_011538405.1:p.Pro136ThrfsTer13
XM_011540104.1:c.405dup	XP_011538406.1:p.Pro136ThrfsTer13
XM_011540103.2:c.405dup	XP_011538405.1:p.Pro136ThrfsTer13
XM_011540104.2:c.405dup	XP_011538406.1:p.Pro136ThrfsTer13
NM_004329.3:c.405dup MANE Select	NP_004320.2:p.Pro136ThrfsTer13