Canonical Allele Identifier: CA377446227

Gene: BMPR1A

Linked Data

• MyVariant Identifiers: chr10:g.88649824A>G (hg19) ; chr10:g.86890067A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.86890067A>G , CM000672.2:g.86890067A>G	GRCh38
NC_000010.10:g.88649824A>G , CM000672.1:g.88649824A>G	GRCh37
NC_000010.9:g.88639804A>G	NCBI36
NG_009362.1:g.138429A>G , LRG_298:g.138429A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000480152.3:c.73A>G	ENSP00000483569.2:p.Asn25Asp
ENST00000635816.2:c.73A>G	ENSP00000489707.1:p.Asn25Asp
ENST00000636056.2:c.73A>G	ENSP00000490273.1:p.Asn25Asp
ENST00000372037.8:c.73A>G MANE Select	ENSP00000361107.2:p.Asn25Asp
ENST00000635816.1:c.73A>G	ENSP00000489707.1:p.Asn25Asp
ENST00000636056.1:c.73A>G	ENSP00000490273.1:p.Asn25Asp
ENST00000638429.1:c.73A>G	ENSP00000492290.1:p.Asn25Asp
ENST00000372037.7:c.73A>G	ENSP00000361107.1:p.Asn25Asp
ENST00000480152.2:c.73A>G	ENSP00000483569.1:p.Asn25Asp
NM_004329.2:c.73A>G , LRG_298t1:c.73A>G	NP_004320.2:p.Asn25Asp
XM_011540103.1:c.73A>G	XP_011538405.1:p.Asn25Asp
XM_011540104.1:c.73A>G	XP_011538406.1:p.Asn25Asp
XM_011540103.2:c.73A>G	XP_011538405.1:p.Asn25Asp
XM_011540104.2:c.73A>G	XP_011538406.1:p.Asn25Asp
NM_004329.3:c.73A>G MANE Select	NP_004320.2:p.Asn25Asp