Canonical Allele Identifier: CA2580082107

Gene: BMPR1A

Linked Data

• ClinVar Variation Id: 2054464
• ClinVar RCV Id: RCV002909787

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86899884_86899886del , CM000672.2:g.86899884_86899886del	GRCh38
NC_000010.10:g.88659641_88659643del , CM000672.1:g.88659641_88659643del	GRCh37
NC_000010.9:g.88649621_88649623del	NCBI36
NG_009362.1:g.148246_148248del , LRG_298:g.148246_148248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.424_426del	ENSP00000483569.2:p.Val142del
ENST00000635816.2:c.424_426del	ENSP00000489707.1:p.Val142del
ENST00000636056.2:c.424_426del	ENSP00000490273.1:p.Val142del
ENST00000372037.8:c.424_426del MANE Select	ENSP00000361107.2:p.Val142del
ENST00000635816.1:c.424_426del	ENSP00000489707.1:p.Val142del
ENST00000636056.1:c.424_426del	ENSP00000490273.1:p.Val142del
ENST00000638429.1:c.424_426del	ENSP00000492290.1:p.Val142del
ENST00000372037.7:c.424_426del	ENSP00000361107.1:p.Val142del
NM_004329.2:c.424_426del , LRG_298t1:c.424_426del	NP_004320.2:p.Val142del
XM_011540103.1:c.424_426del	XP_011538405.1:p.Val142del
XM_011540104.1:c.424_426del	XP_011538406.1:p.Val142del
XM_011540103.2:c.424_426del	XP_011538405.1:p.Val142del
XM_011540104.2:c.424_426del	XP_011538406.1:p.Val142del
NM_004329.3:c.424_426del MANE Select	NP_004320.2:p.Val142del