Canonical Allele Identifier: CA1477952009
Gene: BMPR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.95114642_95114643delinsCT , CM000666.2:g.95114642_95114643delinsCT GRCh38
NC_000004.11:g.96035793_96035794delinsCT , CM000666.1:g.96035793_96035794delinsCT GRCh37
NC_000004.10:g.96254816_96254817delinsCT NCBI36
NG_009245.1:g.361666_361667delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000440890.7:c.234-78_234-77delinsCT ENSP00000401907.2:n.234-78_234-77delinsCT
ENST00000502683.6:n.355-78_355-77delinsCT
ENST00000509540.6:c.144-78_144-77delinsCT ENSP00000421671.1:n.144-78_144-77delinsCT
ENST00000515059.6:c.144-78_144-77delinsCT MANE Select ENSP00000426617.1:n.144-78_144-77delinsCT
ENST00000672698.1:c.144-78_144-77delinsCT ENSP00000500035.1:n.144-78_144-77delinsCT
ENST00000264568.8:c.144-78_144-77delinsCT ENSP00000264568.4:n.144-78_144-77delinsCT
ENST00000394931.1:c.144-78_144-77delinsCT ENSP00000378389.1:n.144-78_144-77delinsCT
ENST00000440890.6:c.234-78_234-77delinsCT ENSP00000401907.2:n.234-78_234-77delinsCT
ENST00000502683.5:c.144-78_144-77delinsCT ENSP00000424693.1:n.144-78_144-77delinsCT
ENST00000506363.5:c.144-78_144-77delinsCT ENSP00000421144.1:n.144-78_144-77delinsCT
ENST00000509540.5:c.144-78_144-77delinsCT ENSP00000421671.1:n.144-78_144-77delinsCT
ENST00000512312.5:c.144-78_144-77delinsCT ENSP00000425444.1:n.144-78_144-77delinsCT
ENST00000515059.5:c.144-78_144-77delinsCT ENSP00000426617.1:n.144-78_144-77delinsCT
NM_001203.2:c.144-78_144-77delinsCT NP_001194.1:n.144-78_144-77delinsCT
NM_001256792.1:c.144-78_144-77delinsCT NP_001243721.1:n.144-78_144-77delinsCT
NM_001256793.1:c.234-78_234-77delinsCT NP_001243722.1:n.234-78_234-77delinsCT
NM_001256794.1:c.144-78_144-77delinsCT NP_001243723.1:n.144-78_144-77delinsCT
XM_011532201.1:c.144-78_144-77delinsCT XP_011530503.1:n.144-78_144-77delinsCT
XM_011532202.1:c.144-78_144-77delinsCT XP_011530504.1:n.144-78_144-77delinsCT
XM_011532201.2:c.144-78_144-77delinsCT XP_011530503.1:n.144-78_144-77delinsCT
XM_017008558.1:c.144-78_144-77delinsCT XP_016864047.1:n.144-78_144-77delinsCT
XM_017008559.1:c.144-78_144-77delinsCT XP_016864048.1:n.144-78_144-77delinsCT
XM_017008560.1:c.144-78_144-77delinsCT XP_016864049.1:n.144-78_144-77delinsCT
XM_017008561.1:c.144-78_144-77delinsCT XP_016864050.1:n.144-78_144-77delinsCT
NM_001203.3:c.144-78_144-77delinsCT MANE Select NP_001194.1:n.144-78_144-77delinsCT
NM_001256793.2:c.234-78_234-77delinsCT NP_001243722.1:n.234-78_234-77delinsCT
NM_001256792.2:c.144-78_144-77delinsCT NP_001243721.1:n.144-78_144-77delinsCT