Canonical Allele Identifier: CA492164773

Gene: BLM

Linked Data

• ClinVar Variation Id: 794765
• ClinVar RCV Id: RCV001413171
• dbSNP Id: rs1596260028
• MyVariant Identifiers: chr15:g.91337518A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90794288A>G , CM000677.2:g.90794288A>G	GRCh38
NC_000015.9:g.91337518A>G , CM000677.1:g.91337518A>G	GRCh37
NC_000015.8:g.89138522A>G	NCBI36
NG_007272.1:g.81917A>G , LRG_20:g.81917A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3141A>G MANE Select	ENSP00000347232.3:p.Glu1047=
ENST00000560559.2:n.1714A>G
ENST00000648453.1:c.3141A>G	ENSP00000497646.1:p.Glu1047=
ENST00000680772.1:c.3141A>G	ENSP00000506117.1:p.Glu1047=
ENST00000681142.1:c.3141A>G	ENSP00000506682.1:p.Glu1047=
ENST00000355112.7:c.3141A>G	ENSP00000347232.3:p.Glu1047=
ENST00000558825.5:n.488A>G
ENST00000559724.5:c.*2065A>G	ENSP00000453359.1:n.*2065A>G
ENST00000560136.5:n.1167A>G
ENST00000560509.5:c.3141A>G	ENSP00000454158.1:p.Glu1047=
ENST00000560559.1:n.678A>G
NM_000057.3:c.3141A>G	NP_000048.1:p.Glu1047=
NM_001287246.1:c.3141A>G	NP_001274175.1:p.Glu1047=
NM_001287247.1:c.3141A>G	NP_001274176.1:p.Glu1047=
NM_001287248.1:c.2016A>G	NP_001274177.1:p.Glu672=
XM_006720632.2:c.1179A>G	XP_006720695.1:p.Glu393=
XM_011521881.1:c.1827A>G	XP_011520183.1:p.Glu609=
XM_011521881.2:c.1827A>G	XP_011520183.1:p.Glu609=
NM_000057.4:c.3141A>G MANE Select	NP_000048.1:p.Glu1047=
NM_001287246.2:c.3141A>G	NP_001274175.1:p.Glu1047=
NM_001287247.2:c.3141A>G	NP_001274176.1:p.Glu1047=
NM_001287248.2:c.2016A>G	NP_001274177.1:p.Glu672=