Canonical Allele Identifier: CA492157865

Gene: BLM

Linked Data

• ClinVar Variation Id: 1127200
• ClinVar RCV Id: RCV001459521
• dbSNP Id: rs1449845656
• gnomAD v2: 15-91354565-G-A
• gnomAD v4: 15-90811335-G-A
• MyVariant Identifiers: chr15:g.91354565G>A (hg19) ; chr15:g.90811335G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811335G>A , CM000677.2:g.90811335G>A	GRCh38
NC_000015.9:g.91354565G>A , CM000677.1:g.91354565G>A	GRCh37
NC_000015.8:g.89155569G>A	NCBI36
NG_007272.1:g.98964G>A , LRG_20:g.98964G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355112.8:c.4005G>A MANE Select	ENSP00000347232.3:p.Lys1335=
ENST00000560559.2:n.2578G>A
ENST00000648453.1:c.4005G>A	ENSP00000497646.1:p.Lys1335=
ENST00000680772.1:c.4005G>A	ENSP00000506117.1:p.Lys1335=
ENST00000681142.1:c.4005G>A	ENSP00000506682.1:p.Lys1335=
ENST00000355112.7:c.4005G>A	ENSP00000347232.3:p.Lys1335=
ENST00000558825.5:n.1352G>A
ENST00000559724.5:c.*2929G>A	ENSP00000453359.1:n.*2929G>A
ENST00000560509.5:c.3612G>A	ENSP00000454158.1:p.Lys1204=
ENST00000560821.1:n.425G>A
NM_000057.3:c.4005G>A	NP_000048.1:p.Lys1335=
NM_001287246.1:c.4005G>A	NP_001274175.1:p.Lys1335=
NM_001287247.1:c.3612G>A	NP_001274176.1:p.Lys1204=
NM_001287248.1:c.2880G>A	NP_001274177.1:p.Lys960=
XM_006720632.2:c.2043G>A	XP_006720695.1:p.Lys681=
XM_011521881.1:c.2691G>A	XP_011520183.1:p.Lys897=
XM_011521881.2:c.2691G>A	XP_011520183.1:p.Lys897=
NM_000057.4:c.4005G>A MANE Select	NP_000048.1:p.Lys1335=
NM_001287246.2:c.4005G>A	NP_001274175.1:p.Lys1335=
NM_001287247.2:c.3612G>A	NP_001274176.1:p.Lys1204=
NM_001287248.2:c.2880G>A	NP_001274177.1:p.Lys960=