Canonical Allele Identifier: CA2609985636

Gene: BMPR1A

Linked Data

• ClinVar Variation Id: 2882826
• ClinVar RCV Id: RCV003763556
• gnomAD v4: 10-86890047-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86890048del , CM000672.2:g.86890048del	GRCh38
NC_000010.10:g.88649805del , CM000672.1:g.88649805del	GRCh37
NC_000010.9:g.88639785del	NCBI36
NG_009362.1:g.138410del , LRG_298:g.138410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.68-14del	ENSP00000483569.2:n.68-14del
ENST00000635816.2:c.68-14del	ENSP00000489707.1:n.68-14del
ENST00000636056.2:c.68-14del	ENSP00000490273.1:n.68-14del
ENST00000372037.8:c.68-14del MANE Select	ENSP00000361107.2:n.68-14del
ENST00000635816.1:c.68-14del	ENSP00000489707.1:n.68-14del
ENST00000636056.1:c.68-14del	ENSP00000490273.1:n.68-14del
ENST00000638429.1:c.68-14del	ENSP00000492290.1:n.68-14del
ENST00000372037.7:c.68-14del	ENSP00000361107.1:n.68-14del
ENST00000480152.2:c.68-14del	ENSP00000483569.1:n.68-14del
NM_004329.2:c.68-14del , LRG_298t1:c.68-14del	NP_004320.2:n.68-14del
XM_011540103.1:c.68-14del	XP_011538405.1:n.68-14del
XM_011540104.1:c.68-14del	XP_011538406.1:n.68-14del
XM_011540103.2:c.68-14del	XP_011538405.1:n.68-14del
XM_011540104.2:c.68-14del	XP_011538406.1:n.68-14del
NM_004329.3:c.68-14del MANE Select	NP_004320.2:n.68-14del