Canonical Allele Identifier: CA918724616

Gene: BMPR1A

Linked Data

• dbSNP Id: rs1589700546

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86757299dup , CM000672.2:g.86757299dup	GRCh38
NC_000010.10:g.88517056dup , CM000672.1:g.88517056dup	GRCh37
NC_000010.9:g.88507036dup	NCBI36
NG_009362.1:g.5661dup , LRG_298:g.5661dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-373+380dup	ENSP00000483569.2:n.-373+380dup
ENST00000635816.2:c.-268+380dup	ENSP00000489707.1:n.-268+380dup
ENST00000636056.2:c.-268+380dup	ENSP00000490273.1:n.-268+380dup
ENST00000372037.8:c.-268+380dup MANE Select	ENSP00000361107.2:n.-268+380dup
ENST00000638429.1:c.-268+380dup	ENSP00000492290.1:n.-268+380dup
ENST00000372037.7:c.-268+380dup	ENSP00000361107.1:n.-268+380dup
NM_004329.2:c.-268+380dup , LRG_298t1:c.-268+380dup	NP_004320.2:n.-268+380dup
XM_011540103.1:c.-268+1336dup	XP_011538405.1:n.-268+1336dup
XM_011540104.1:c.-373+380dup	XP_011538406.1:n.-373+380dup
XM_011540103.2:c.-268+1336dup	XP_011538405.1:n.-268+1336dup
XM_011540104.2:c.-373+380dup	XP_011538406.1:n.-373+380dup
NM_004329.3:c.-268+380dup MANE Select	NP_004320.2:n.-268+380dup