Canonical Allele Identifier: CA1925653719

Gene: BMPR1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86757278T= , CM000672.2:g.86757278T=	GRCh38
NC_000010.10:g.88517035T= , CM000672.1:g.88517035T=	GRCh37
NC_000010.9:g.88507015T=	NCBI36
NG_009362.1:g.5640T= , LRG_298:g.5640T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-373+359T=	ENSP00000483569.2:n.-373+359T=
ENST00000635816.2:c.-268+359T=	ENSP00000489707.1:n.-268+359T=
ENST00000636056.2:c.-268+359T=	ENSP00000490273.1:n.-268+359T=
ENST00000372037.8:c.-268+359T= MANE Select	ENSP00000361107.2:n.-268+359T=
ENST00000638429.1:c.-268+359T=	ENSP00000492290.1:n.-268+359T=
ENST00000372037.7:c.-268+359T=	ENSP00000361107.1:n.-268+359T=
NM_004329.2:c.-268+359T= , LRG_298t1:c.-268+359T=	NP_004320.2:n.-268+359T=
XM_011540103.1:c.-268+1315T=	XP_011538405.1:n.-268+1315T=
XM_011540104.1:c.-373+359T=	XP_011538406.1:n.-373+359T=
XM_011540103.2:c.-268+1315T=	XP_011538405.1:n.-268+1315T=
XM_011540104.2:c.-373+359T=	XP_011538406.1:n.-373+359T=
NM_004329.3:c.-268+359T= MANE Select	NP_004320.2:n.-268+359T=