Canonical Allele Identifier: CA1925707212
Gene: BMPR1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86876124_86876126delinsTAA , CM000672.2:g.86876124_86876126delinsTAA GRCh38
NC_000010.10:g.88635881_88635883delinsTAA , CM000672.1:g.88635881_88635883delinsTAA GRCh37
NC_000010.9:g.88625861_88625863delinsTAA NCBI36
NG_009362.1:g.124486_124488delinsTAA , LRG_298:g.124486_124488delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.67+39_67+41delinsTAA ENSP00000483569.2:n.67+39_67+41delinsTAA
ENST00000635816.2:c.67+39_67+41delinsTAA ENSP00000489707.1:n.67+39_67+41delinsTAA
ENST00000636056.2:c.67+39_67+41delinsTAA ENSP00000490273.1:n.67+39_67+41delinsTAA
ENST00000372037.8:c.67+39_67+41delinsTAA MANE Select ENSP00000361107.2:n.67+39_67+41delinsTAA
ENST00000635816.1:c.67+39_67+41delinsTAA ENSP00000489707.1:n.67+39_67+41delinsTAA
ENST00000636056.1:c.67+39_67+41delinsTAA ENSP00000490273.1:n.67+39_67+41delinsTAA
ENST00000638429.1:c.67+39_67+41delinsTAA ENSP00000492290.1:n.67+39_67+41delinsTAA
ENST00000372037.7:c.67+39_67+41delinsTAA ENSP00000361107.1:n.67+39_67+41delinsTAA
ENST00000480152.2:c.67+39_67+41delinsTAA ENSP00000483569.1:n.67+39_67+41delinsTAA
NM_004329.2:c.67+39_67+41delinsTAA , LRG_298t1:c.67+39_67+41delinsTAA NP_004320.2:n.67+39_67+41delinsTAA
XM_011540103.1:c.67+39_67+41delinsTAA XP_011538405.1:n.67+39_67+41delinsTAA
XM_011540104.1:c.67+39_67+41delinsTAA XP_011538406.1:n.67+39_67+41delinsTAA
XM_011540103.2:c.67+39_67+41delinsTAA XP_011538405.1:n.67+39_67+41delinsTAA
XM_011540104.2:c.67+39_67+41delinsTAA XP_011538406.1:n.67+39_67+41delinsTAA
NM_004329.3:c.67+39_67+41delinsTAA MANE Select NP_004320.2:n.67+39_67+41delinsTAA