Canonical Allele Identifier: CA370543203

Gene: BMP1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22177868C>A , CM000670.2:g.22177868C>A	GRCh38
NC_000008.10:g.22035381C>A , CM000670.1:g.22035381C>A	GRCh37
NC_000008.9:g.22091326C>A	NCBI36
NG_029659.1:g.17729C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306349.13:c.747C>A MANE Plus Clinical	ENSP00000306121.8:p.Phe249Leu
ENST00000306385.10:c.747C>A MANE Select	ENSP00000305714.5:p.Phe249Leu
ENST00000520626.6:c.*594C>A	ENSP00000430015.2:n.*594C>A
ENST00000306349.12:c.747C>A	ENSP00000306121.8:p.Phe249Leu
ENST00000306385.9:c.747C>A	ENSP00000305714.5:p.Phe249Leu
ENST00000354870.5:c.*4C>A	ENSP00000346941.5:n.*4C>A
ENST00000471755.5:c.747C>A	ENSP00000428665.1:p.Phe249Leu
ENST00000483364.5:c.*4C>A	ENSP00000428249.1:n.*4C>A
ENST00000518656.5:c.*380C>A	ENSP00000430977.1:n.*380C>A
ENST00000518913.5:c.*214C>A	ENSP00000427950.1:n.*214C>A
ENST00000520626.5:c.*594C>A	ENSP00000430015.1:n.*594C>A
ENST00000520970.5:c.747C>A	ENSP00000428332.1:p.Phe249Leu
ENST00000520982.5:c.*214C>A	ENSP00000428798.1:n.*214C>A
ENST00000521385.5:c.747C>A	ENSP00000430406.1:p.Phe249Leu
NM_001199.3:c.747C>A	NP_001190.1:p.Phe249Leu
NM_006129.4:c.747C>A	NP_006120.1:p.Phe249Leu
NR_033403.1:n.1050C>A
NR_033404.1:n.1050C>A
XM_006716386.2:c.747C>A	XP_006716449.2:p.Phe249Leu
XM_011544617.1:c.747C>A	XP_011542919.1:p.Phe249Leu
XR_428315.2:n.1013C>A
XR_949458.1:n.1013C>A
XM_006716386.3:c.747C>A	XP_006716449.2:p.Phe249Leu
XM_011544617.2:c.747C>A	XP_011542919.1:p.Phe249Leu
XM_017013738.2:c.747C>A	XP_016869227.1:p.Phe249Leu
XR_001745579.2:n.955C>A
XR_949458.2:n.955C>A
NM_006129.5:c.747C>A MANE Select	NP_006120.1:p.Phe249Leu
NM_001199.4:c.747C>A MANE Plus Clinical	NP_001190.1:p.Phe249Leu
NR_033403.2:n.818C>A
NR_033404.2:n.818C>A