Canonical Allele Identifier: CA2610001671
Gene: BMPR1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.86917099_86917101del , CM000672.2:g.86917099_86917101del GRCh38
NC_000010.10:g.88676856_88676858del , CM000672.1:g.88676856_88676858del GRCh37
NC_000010.9:g.88666836_88666838del NCBI36
NG_009362.1:g.165461_165463del , LRG_298:g.165461_165463del

Transcript Alleles

HGVS Amino-acid Change
ENST00000480152.3:c.676-35_676-33del ENSP00000483569.2:n.676-35_676-33del
ENST00000635816.2:c.676-35_676-33del ENSP00000489707.1:n.676-35_676-33del
ENST00000636056.2:c.676-35_676-33del ENSP00000490273.1:n.676-35_676-33del
ENST00000372037.8:c.676-35_676-33del MANE Select ENSP00000361107.2:n.676-35_676-33del
ENST00000635816.1:c.676-35_676-33del ENSP00000489707.1:n.676-35_676-33del
ENST00000636056.1:c.676-35_676-33del ENSP00000490273.1:n.676-35_676-33del
ENST00000638429.1:c.676-35_676-33del ENSP00000492290.1:n.676-35_676-33del
ENST00000372037.7:c.676-35_676-33del ENSP00000361107.1:n.676-35_676-33del
NM_004329.2:c.676-35_676-33del , LRG_298t1:c.676-35_676-33del NP_004320.2:n.676-35_676-33del
XM_011540103.1:c.676-35_676-33del XP_011538405.1:n.676-35_676-33del
XM_011540104.1:c.676-35_676-33del XP_011538406.1:n.676-35_676-33del
XM_011540103.2:c.676-35_676-33del XP_011538405.1:n.676-35_676-33del
XM_011540104.2:c.676-35_676-33del XP_011538406.1:n.676-35_676-33del
NM_004329.3:c.676-35_676-33del MANE Select NP_004320.2:n.676-35_676-33del