Canonical Allele Identifier: CA377446323

Gene: BMPR1A

Linked Data

• ClinVar Variation Id: 640801
• ClinVar RCV Id: RCV001766631
• dbSNP Id: rs1589763313
• MyVariant Identifiers: chr10:g.88649843A>C (hg19) ; chr10:g.86890086A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86890086A>C , CM000672.2:g.86890086A>C	GRCh38
NC_000010.10:g.88649843A>C , CM000672.1:g.88649843A>C	GRCh37
NC_000010.9:g.88639823A>C	NCBI36
NG_009362.1:g.138448A>C , LRG_298:g.138448A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000480152.3:c.92A>C	ENSP00000483569.2:p.His31Pro
ENST00000635816.2:c.92A>C	ENSP00000489707.1:p.His31Pro
ENST00000636056.2:c.92A>C	ENSP00000490273.1:p.His31Pro
ENST00000372037.8:c.92A>C MANE Select	ENSP00000361107.2:p.His31Pro
ENST00000635816.1:c.92A>C	ENSP00000489707.1:p.His31Pro
ENST00000636056.1:c.92A>C	ENSP00000490273.1:p.His31Pro
ENST00000638429.1:c.92A>C	ENSP00000492290.1:p.His31Pro
ENST00000372037.7:c.92A>C	ENSP00000361107.1:p.His31Pro
ENST00000480152.2:c.92A>C	ENSP00000483569.1:p.His31Pro
NM_004329.2:c.92A>C , LRG_298t1:c.92A>C	NP_004320.2:p.His31Pro
XM_011540103.1:c.92A>C	XP_011538405.1:p.His31Pro
XM_011540104.1:c.92A>C	XP_011538406.1:p.His31Pro
XM_011540103.2:c.92A>C	XP_011538405.1:p.His31Pro
XM_011540104.2:c.92A>C	XP_011538406.1:p.His31Pro
NM_004329.3:c.92A>C MANE Select	NP_004320.2:p.His31Pro