Canonical Allele Identifier: CA393850921

Gene: BLM

Linked Data

• ClinVar Variation Id: 1736550
• ClinVar RCV Id: RCV002357700
• MyVariant Identifiers: chr15:g.91354525C>A (hg19) ; chr15:g.90811295C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811295C>A , CM000677.2:g.90811295C>A	GRCh38
NC_000015.9:g.91354525C>A , CM000677.1:g.91354525C>A	GRCh37
NC_000015.8:g.89155529C>A	NCBI36
NG_007272.1:g.98924C>A , LRG_20:g.98924C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3965C>A MANE Select	ENSP00000347232.3:p.Ser1322Tyr
ENST00000560559.2:n.2538C>A
ENST00000648453.1:c.3965C>A	ENSP00000497646.1:p.Ser1322Tyr
ENST00000680772.1:c.3965C>A	ENSP00000506117.1:p.Ser1322Tyr
ENST00000681142.1:c.3965C>A	ENSP00000506682.1:p.Ser1322Tyr
ENST00000355112.7:c.3965C>A	ENSP00000347232.3:p.Ser1322Tyr
ENST00000558825.5:n.1312C>A
ENST00000559724.5:c.*2889C>A	ENSP00000453359.1:n.*2889C>A
ENST00000560136.5:n.1991C>A
ENST00000560509.5:c.3572C>A	ENSP00000454158.1:p.Ser1191Tyr
ENST00000560821.1:n.385C>A
NM_000057.3:c.3965C>A	NP_000048.1:p.Ser1322Tyr
NM_001287246.1:c.3965C>A	NP_001274175.1:p.Ser1322Tyr
NM_001287247.1:c.3572C>A	NP_001274176.1:p.Ser1191Tyr
NM_001287248.1:c.2840C>A	NP_001274177.1:p.Ser947Tyr
XM_006720632.2:c.2003C>A	XP_006720695.1:p.Ser668Tyr
XM_011521881.1:c.2651C>A	XP_011520183.1:p.Ser884Tyr
XM_011521881.2:c.2651C>A	XP_011520183.1:p.Ser884Tyr
NM_000057.4:c.3965C>A MANE Select	NP_000048.1:p.Ser1322Tyr
NM_001287246.2:c.3965C>A	NP_001274175.1:p.Ser1322Tyr
NM_001287247.2:c.3572C>A	NP_001274176.1:p.Ser1191Tyr
NM_001287248.2:c.2840C>A	NP_001274177.1:p.Ser947Tyr