Canonical Allele Identifier: CA669480569

Gene: BMPR1A

Linked Data

• dbSNP Id: rs1284269226
• MyVariant Identifiers: chr10:g.88516575_88516607del (hg19) ; chr10:g.86756818_86756850del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86756822_86756854del , CM000672.2:g.86756822_86756854del	GRCh38
NC_000010.10:g.88516579_88516611del , CM000672.1:g.88516579_88516611del	GRCh37
NC_000010.9:g.88506559_88506591del	NCBI36
NG_009362.1:g.5184_5216del , LRG_298:g.5184_5216del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.-470_-438del	ENSP00000483569.2:n.-470_-438del
ENST00000635816.2:c.-365_-333del	ENSP00000489707.1:n.-365_-333del
ENST00000636056.2:c.-365_-333del	ENSP00000490273.1:n.-365_-333del
ENST00000372037.8:c.-365_-333del MANE Select	ENSP00000361107.2:n.-365_-333del
ENST00000638429.1:c.-365_-333del	ENSP00000492290.1:n.-365_-333del
ENST00000372037.7:c.-365_-333del	ENSP00000361107.1:n.-365_-333del
NM_004329.2:c.-365_-333del , LRG_298t1:c.-365_-333del	NP_004320.2:n.-365_-333del
XM_011540103.1:c.-268+859_-268+891del	XP_011538405.1:n.-268+859_-268+891del
XM_011540104.1:c.-470_-438del	XP_011538406.1:n.-470_-438del
XM_011540103.2:c.-268+859_-268+891del	XP_011538405.1:n.-268+859_-268+891del
XM_011540104.2:c.-470_-438del	XP_011538406.1:n.-470_-438del
NM_004329.3:c.-365_-333del MANE Select	NP_004320.2:n.-365_-333del