Canonical Allele Identifier: CA211238841

Gene: BMPR1A

Linked Data

• dbSNP Id: rs751434732
• MyVariant Identifiers: chr10:g.88635870_88635871insT (hg19) ; chr10:g.86876113_86876114insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86876114dup , CM000672.2:g.86876114dup	GRCh38
NC_000010.10:g.88635871dup , CM000672.1:g.88635871dup	GRCh37
NC_000010.9:g.88625851dup	NCBI36
NG_009362.1:g.124476dup , LRG_298:g.124476dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000480152.3:c.67+29dup	ENSP00000483569.2:n.67+29dup
ENST00000635816.2:c.67+29dup	ENSP00000489707.1:n.67+29dup
ENST00000636056.2:c.67+29dup	ENSP00000490273.1:n.67+29dup
ENST00000372037.8:c.67+29dup MANE Select	ENSP00000361107.2:n.67+29dup
ENST00000635816.1:c.67+29dup	ENSP00000489707.1:n.67+29dup
ENST00000636056.1:c.67+29dup	ENSP00000490273.1:n.67+29dup
ENST00000638429.1:c.67+29dup	ENSP00000492290.1:n.67+29dup
ENST00000372037.7:c.67+29dup	ENSP00000361107.1:n.67+29dup
ENST00000480152.2:c.67+29dup	ENSP00000483569.1:n.67+29dup
NM_004329.2:c.67+29dup , LRG_298t1:c.67+29dup	NP_004320.2:n.67+29dup
XM_011540103.1:c.67+29dup	XP_011538405.1:n.67+29dup
XM_011540104.1:c.67+29dup	XP_011538406.1:n.67+29dup
XM_011540103.2:c.67+29dup	XP_011538405.1:n.67+29dup
XM_011540104.2:c.67+29dup	XP_011538406.1:n.67+29dup
NM_004329.3:c.67+29dup MANE Select	NP_004320.2:n.67+29dup