Canonical Allele Identifier: CA1770294922

Gene: BMP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22201462G= , CM000670.2:g.22201462G=	GRCh38
NC_000008.10:g.22058975G= , CM000670.1:g.22058975G=	GRCh37
NC_000008.9:g.22114920G=	NCBI36
NG_029659.1:g.41323G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306349.13:c.*259G= MANE Plus Clinical	ENSP00000306121.8:n.*259G=
ENST00000306385.10:c.2108-341G= MANE Select	ENSP00000305714.5:n.2108-341G=
ENST00000520626.6:c.*2299G=	ENSP00000430015.2:n.*2299G=
ENST00000306349.12:c.*259G=	ENSP00000306121.8:n.*259G=
ENST00000306385.9:c.2108-341G=	ENSP00000305714.5:n.2108-341G=
ENST00000354870.5:c.*1365-341G=	ENSP00000346941.5:n.*1365-341G=
ENST00000518913.5:c.*1919G=	ENSP00000427950.1:n.*1919G=
ENST00000520626.5:c.*2299G=	ENSP00000430015.1:n.*2299G=
ENST00000520970.5:c.*259G=	ENSP00000428332.1:n.*259G=
ENST00000520982.5:c.*1575-341G=	ENSP00000428798.1:n.*1575-341G=
ENST00000522332.1:n.1317G=
NM_001199.3:c.*259G=	NP_001190.1:n.*259G=
NM_006129.4:c.2108-341G=	NP_006120.1:n.2108-341G=
NR_033403.1:n.2411-341G=
NR_033404.1:n.2755G=
XR_949458.1:n.2481-341G=
XR_001745579.2:n.2660G=
XR_949458.2:n.2423-341G=
NM_006129.5:c.2108-341G= MANE Select	NP_006120.1:n.2108-341G=
NM_001199.4:c.*259G= MANE Plus Clinical	NP_001190.1:n.*259G=
NR_033403.2:n.2179-341G=
NR_033404.2:n.2523G=