Canonical Allele Identifier: CA580546649
Gene: BMP1 HGNC NCBI

Linked Data

dbSNP Id: rs1389323439

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22177772del , CM000670.2:g.22177772del GRCh38
NC_000008.10:g.22035285del , CM000670.1:g.22035285del GRCh37
NC_000008.9:g.22091230del NCBI36
NG_029659.1:g.17633del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306349.13:c.731-80del MANE Plus Clinical ENSP00000306121.8:n.731-80del
ENST00000306385.10:c.731-80del MANE Select ENSP00000305714.5:n.731-80del
ENST00000520626.6:c.*578-80del ENSP00000430015.2:n.*578-80del
ENST00000306349.12:c.731-80del ENSP00000306121.8:n.731-80del
ENST00000306385.9:c.731-80del ENSP00000305714.5:n.731-80del
ENST00000354870.5:c.896+40del ENSP00000346941.5:n.896+40del
ENST00000471755.5:c.731-80del ENSP00000428665.1:n.731-80del
ENST00000483364.5:c.896+40del ENSP00000428249.1:n.896+40del
ENST00000518656.5:c.*363+40del ENSP00000430977.1:n.*363+40del
ENST00000518913.5:c.*198-80del ENSP00000427950.1:n.*198-80del
ENST00000520626.5:c.*578-80del ENSP00000430015.1:n.*578-80del
ENST00000520970.5:c.731-80del ENSP00000428332.1:n.731-80del
ENST00000520982.5:c.*198-80del ENSP00000428798.1:n.*198-80del
ENST00000521385.5:c.731-80del ENSP00000430406.1:n.731-80del
NM_001199.3:c.731-80del NP_001190.1:n.731-80del
NM_006129.4:c.731-80del NP_006120.1:n.731-80del
NR_033403.1:n.1034-80del
NR_033404.1:n.1034-80del
XM_006716386.2:c.731-80del XP_006716449.2:n.731-80del
XM_011544617.1:c.731-80del XP_011542919.1:n.731-80del
XR_428315.2:n.997-80del
XR_949458.1:n.997-80del
XM_006716386.3:c.731-80del XP_006716449.2:n.731-80del
XM_011544617.2:c.731-80del XP_011542919.1:n.731-80del
XM_017013738.2:c.731-80del XP_016869227.1:n.731-80del
XR_001745579.2:n.939-80del
XR_949458.2:n.939-80del
NM_006129.5:c.731-80del MANE Select NP_006120.1:n.731-80del
NM_001199.4:c.731-80del MANE Plus Clinical NP_001190.1:n.731-80del
NR_033403.2:n.802-80del
NR_033404.2:n.802-80del