Canonical Allele Identifier: CA1925653743

Gene: BMPR1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86757302G= , CM000672.2:g.86757302G=	GRCh38
NC_000010.10:g.88517059G= , CM000672.1:g.88517059G=	GRCh37
NC_000010.9:g.88507039G=	NCBI36
NG_009362.1:g.5664G= , LRG_298:g.5664G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-373+383G=	ENSP00000483569.2:n.-373+383G=
ENST00000635816.2:c.-268+383G=	ENSP00000489707.1:n.-268+383G=
ENST00000636056.2:c.-268+383G=	ENSP00000490273.1:n.-268+383G=
ENST00000372037.8:c.-268+383G= MANE Select	ENSP00000361107.2:n.-268+383G=
ENST00000638429.1:c.-268+383G=	ENSP00000492290.1:n.-268+383G=
ENST00000372037.7:c.-268+383G=	ENSP00000361107.1:n.-268+383G=
NM_004329.2:c.-268+383G= , LRG_298t1:c.-268+383G=	NP_004320.2:n.-268+383G=
XM_011540103.1:c.-268+1339G=	XP_011538405.1:n.-268+1339G=
XM_011540104.1:c.-373+383G=	XP_011538406.1:n.-373+383G=
XM_011540103.2:c.-268+1339G=	XP_011538405.1:n.-268+1339G=
XM_011540104.2:c.-373+383G=	XP_011538406.1:n.-373+383G=
NM_004329.3:c.-268+383G= MANE Select	NP_004320.2:n.-268+383G=