Canonical Allele Identifier: CA4664495

Gene: BMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22180350C>G , CM000670.2:g.22180350C>G	GRCh38
NC_000008.10:g.22037863C>G , CM000670.1:g.22037863C>G	GRCh37
NC_000008.9:g.22093808C>G	NCBI36
NG_029659.1:g.20211C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006129.5:c.962-18C>G MANE Select	NP_006120.1:n.962-18C>G
ENST00000306385.10:c.962-18C>G MANE Select	ENSP00000305714.5:n.962-18C>G
NM_001199.4:c.962-18C>G MANE Plus Clinical	NP_001190.1:n.962-18C>G
ENST00000306349.13:c.962-18C>G MANE Plus Clinical	ENSP00000306121.8:n.962-18C>G
NM_001199.3:c.962-18C>G	NP_001190.1:n.962-18C>G
NM_006129.4:c.962-18C>G	NP_006120.1:n.962-18C>G
NR_033403.1:n.1265-18C>G
NR_033403.2:n.1033-18C>G
NR_033404.1:n.1265-18C>G
NR_033404.2:n.1033-18C>G
ENST00000306349.12:c.962-18C>G	ENSP00000306121.8:n.962-18C>G
ENST00000306385.9:c.962-18C>G	ENSP00000305714.5:n.962-18C>G
ENST00000354870.5:c.*219-18C>G	ENSP00000346941.5:n.*219-18C>G
ENST00000471755.5:c.962-18C>G	ENSP00000428665.1:n.962-18C>G
ENST00000483364.5:c.*219-18C>G	ENSP00000428249.1:n.*219-18C>G
ENST00000518913.5:c.*429-18C>G	ENSP00000427950.1:n.*429-18C>G
ENST00000520626.5:c.*809-18C>G	ENSP00000430015.1:n.*809-18C>G
ENST00000520626.6:c.*809-18C>G	ENSP00000430015.2:n.*809-18C>G
ENST00000520970.5:c.962-18C>G	ENSP00000428332.1:n.962-18C>G
ENST00000520982.5:c.*429-18C>G	ENSP00000428798.1:n.*429-18C>G
ENST00000521385.5:c.962-18C>G	ENSP00000430406.1:n.962-18C>G
ENST00000523457.5:n.134-18C>G
XM_006716386.2:c.962-18C>G	XP_006716449.2:n.962-18C>G
XM_006716386.3:c.962-18C>G	XP_006716449.2:n.962-18C>G
XM_011544617.1:c.962-18C>G	XP_011542919.1:n.962-18C>G
XM_011544617.2:c.962-18C>G	XP_011542919.1:n.962-18C>G
XM_017013738.2:c.962-18C>G	XP_016869227.1:n.962-18C>G
XR_001745579.2:n.1170-18C>G
XR_428315.2:n.1228-18C>G
XR_949458.1:n.1228-18C>G
XR_949458.2:n.1170-18C>G