Canonical Allele Identifier: CA1925653553

Gene: BMPR1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86757146C= , CM000672.2:g.86757146C=	GRCh38
NC_000010.10:g.88516903C= , CM000672.1:g.88516903C=	GRCh37
NC_000010.9:g.88506883C=	NCBI36
NG_009362.1:g.5508C= , LRG_298:g.5508C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-373+227C=	ENSP00000483569.2:n.-373+227C=
ENST00000635816.2:c.-268+227C=	ENSP00000489707.1:n.-268+227C=
ENST00000636056.2:c.-268+227C=	ENSP00000490273.1:n.-268+227C=
ENST00000372037.8:c.-268+227C= MANE Select	ENSP00000361107.2:n.-268+227C=
ENST00000638429.1:c.-268+227C=	ENSP00000492290.1:n.-268+227C=
ENST00000372037.7:c.-268+227C=	ENSP00000361107.1:n.-268+227C=
NM_004329.2:c.-268+227C= , LRG_298t1:c.-268+227C=	NP_004320.2:n.-268+227C=
XM_011540103.1:c.-268+1183C=	XP_011538405.1:n.-268+1183C=
XM_011540104.1:c.-373+227C=	XP_011538406.1:n.-373+227C=
XM_011540103.2:c.-268+1183C=	XP_011538405.1:n.-268+1183C=
XM_011540104.2:c.-373+227C=	XP_011538406.1:n.-373+227C=
NM_004329.3:c.-268+227C= MANE Select	NP_004320.2:n.-268+227C=