Canonical Allele Identifier: CA393846352

Gene: BLM

Linked Data

• COSMIC: COSM1629744
• MyVariant Identifiers: chr15:g.91333944T>A (hg19) ; chr15:g.90790714T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90790714T>A , CM000677.2:g.90790714T>A	GRCh38
NC_000015.9:g.91333944T>A , CM000677.1:g.91333944T>A	GRCh37
NC_000015.8:g.89134948T>A	NCBI36
NG_007272.1:g.78343T>A , LRG_20:g.78343T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.2889T>A MANE Select	ENSP00000347232.3:p.His963Gln
ENST00000560559.2:n.1462T>A
ENST00000648453.1:c.2889T>A	ENSP00000497646.1:p.His963Gln
ENST00000680772.1:c.2889T>A	ENSP00000506117.1:p.His963Gln
ENST00000681142.1:c.2889T>A	ENSP00000506682.1:p.His963Gln
ENST00000355112.7:c.2889T>A	ENSP00000347232.3:p.His963Gln
ENST00000559724.5:c.*1813T>A	ENSP00000453359.1:n.*1813T>A
ENST00000560136.5:n.915T>A
ENST00000560509.5:c.2889T>A	ENSP00000454158.1:p.His963Gln
ENST00000560559.1:n.426T>A
NM_000057.3:c.2889T>A	NP_000048.1:p.His963Gln
NM_001287246.1:c.2889T>A	NP_001274175.1:p.His963Gln
NM_001287247.1:c.2889T>A	NP_001274176.1:p.His963Gln
NM_001287248.1:c.1764T>A	NP_001274177.1:p.His588Gln
XM_006720632.2:c.927T>A	XP_006720695.1:p.His309Gln
XM_011521881.1:c.1575T>A	XP_011520183.1:p.His525Gln
XM_011521881.2:c.1575T>A	XP_011520183.1:p.His525Gln
NM_000057.4:c.2889T>A MANE Select	NP_000048.1:p.His963Gln
NM_001287246.2:c.2889T>A	NP_001274175.1:p.His963Gln
NM_001287247.2:c.2889T>A	NP_001274176.1:p.His963Gln
NM_001287248.2:c.1764T>A	NP_001274177.1:p.His588Gln