Canonical Allele Identifier: CA2609985152

Gene: BMPR1A

Linked Data

• gnomAD v4: 10-86875871-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86875872del , CM000672.2:g.86875872del	GRCh38
NC_000010.10:g.88635629del , CM000672.1:g.88635629del	GRCh37
NC_000010.9:g.88625609del	NCBI36
NG_009362.1:g.124234del , LRG_298:g.124234del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-147del	ENSP00000483569.2:n.-147del
ENST00000635816.2:c.-147del	ENSP00000489707.1:n.-147del
ENST00000636056.2:c.-147del	ENSP00000490273.1:n.-147del
ENST00000372037.8:c.-147del MANE Select	ENSP00000361107.2:n.-147del
ENST00000635816.1:c.-147del	ENSP00000489707.1:n.-147del
ENST00000636056.1:c.-147del	ENSP00000490273.1:n.-147del
ENST00000638429.1:c.-147del	ENSP00000492290.1:n.-147del
ENST00000372037.7:c.-147del	ENSP00000361107.1:n.-147del
ENST00000480152.2:c.-147del	ENSP00000483569.1:n.-147del
NM_004329.2:c.-147del , LRG_298t1:c.-147del	NP_004320.2:n.-147del
XM_011540103.1:c.-147del	XP_011538405.1:n.-147del
XM_011540104.1:c.-147del	XP_011538406.1:n.-147del
XM_011540103.2:c.-147del	XP_011538405.1:n.-147del
XM_011540104.2:c.-147del	XP_011538406.1:n.-147del
NM_004329.3:c.-147del MANE Select	NP_004320.2:n.-147del