Canonical Allele Identifier: CA1925706852
Gene: BMPR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86876023C= , CM000672.2:g.86876023C= GRCh38
NC_000010.10:g.88635780C= , CM000672.1:g.88635780C= GRCh37
NC_000010.9:g.88625760C= NCBI36
NG_009362.1:g.124385C= , LRG_298:g.124385C=

Transcript Alleles

HGVS Amino-acid change
ENST00000480152.3:c.5C= ENSP00000483569.2:p.Pro2=
ENST00000635816.2:c.5C= ENSP00000489707.1:p.Pro2=
ENST00000636056.2:c.5C= ENSP00000490273.1:p.Pro2=
ENST00000372037.8:c.5C= MANE Select ENSP00000361107.2:p.Pro2=
ENST00000635816.1:c.5C= ENSP00000489707.1:p.Pro2=
ENST00000636056.1:c.5C= ENSP00000490273.1:p.Pro2=
ENST00000638429.1:c.5C= ENSP00000492290.1:p.Pro2=
ENST00000372037.7:c.5C= ENSP00000361107.1:p.Pro2=
ENST00000480152.2:c.5C= ENSP00000483569.1:p.Pro2=
NM_004329.2:c.5C= , LRG_298t1:c.5C= NP_004320.2:p.Pro2=
XM_011540103.1:c.5C= XP_011538405.1:p.Pro2=
XM_011540104.1:c.5C= XP_011538406.1:p.Pro2=
XM_011540103.2:c.5C= XP_011538405.1:p.Pro2=
XM_011540104.2:c.5C= XP_011538406.1:p.Pro2=
NM_004329.3:c.5C= MANE Select NP_004320.2:p.Pro2=