Canonical Allele Identifier: CA1925692825

Gene: BMPR1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86842759C= , CM000672.2:g.86842759C=	GRCh38
NC_000010.10:g.88602516C= , CM000672.1:g.88602516C=	GRCh37
NC_000010.9:g.88592496C=	NCBI36
NG_009362.1:g.91121C= , LRG_298:g.91121C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-257-647C=	ENSP00000483569.2:n.-257-647C=
ENST00000635816.2:c.-153+3780C=	ENSP00000489707.1:n.-153+3780C=
ENST00000636056.2:c.-153+3780C=	ENSP00000490273.1:n.-153+3780C=
ENST00000372037.8:c.-153+3780C= MANE Select	ENSP00000361107.2:n.-153+3780C=
ENST00000635816.1:c.-153+3780C=	ENSP00000489707.1:n.-153+3780C=
ENST00000636056.1:c.-153+3780C=	ENSP00000490273.1:n.-153+3780C=
ENST00000638429.1:c.-153+3780C=	ENSP00000492290.1:n.-153+3780C=
ENST00000372037.7:c.-153+3780C=	ENSP00000361107.1:n.-153+3780C=
ENST00000480152.2:c.-257-647C=	ENSP00000483569.1:n.-257-647C=
NM_004329.2:c.-153+3780C= , LRG_298t1:c.-153+3780C=	NP_004320.2:n.-153+3780C=
XM_011540103.1:c.-153+3780C=	XP_011538405.1:n.-153+3780C=
XM_011540104.1:c.-257-647C=	XP_011538406.1:n.-257-647C=
XM_011540103.2:c.-153+3780C=	XP_011538405.1:n.-153+3780C=
XM_011540104.2:c.-257-647C=	XP_011538406.1:n.-257-647C=
NM_004329.3:c.-153+3780C= MANE Select	NP_004320.2:n.-153+3780C=