Canonical Allele Identifier: CA393850636

Gene: BLM

Linked Data

• ClinVar Variation Id: 2708856
• ClinVar RCV Id: RCV003505933
• MyVariant Identifiers: chr15:g.91354488A>C (hg19) ; chr15:g.90811258A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811258A>C , CM000677.2:g.90811258A>C	GRCh38
NC_000015.9:g.91354488A>C , CM000677.1:g.91354488A>C	GRCh37
NC_000015.8:g.89155492A>C	NCBI36
NG_007272.1:g.98887A>C , LRG_20:g.98887A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3928A>C MANE Select	ENSP00000347232.3:p.Ser1310Arg
ENST00000560559.2:n.2501A>C
ENST00000648453.1:c.3928A>C	ENSP00000497646.1:p.Ser1310Arg
ENST00000680772.1:c.3928A>C	ENSP00000506117.1:p.Ser1310Arg
ENST00000681142.1:c.3928A>C	ENSP00000506682.1:p.Ser1310Arg
ENST00000355112.7:c.3928A>C	ENSP00000347232.3:p.Ser1310Arg
ENST00000558825.5:n.1275A>C
ENST00000559724.5:c.*2852A>C	ENSP00000453359.1:n.*2852A>C
ENST00000560136.5:n.1954A>C
ENST00000560509.5:c.3535A>C	ENSP00000454158.1:p.Ser1179Arg
ENST00000560821.1:n.348A>C
NM_000057.3:c.3928A>C	NP_000048.1:p.Ser1310Arg
NM_001287246.1:c.3928A>C	NP_001274175.1:p.Ser1310Arg
NM_001287247.1:c.3535A>C	NP_001274176.1:p.Ser1179Arg
NM_001287248.1:c.2803A>C	NP_001274177.1:p.Ser935Arg
XM_006720632.2:c.1966A>C	XP_006720695.1:p.Ser656Arg
XM_011521881.1:c.2614A>C	XP_011520183.1:p.Ser872Arg
XM_011521881.2:c.2614A>C	XP_011520183.1:p.Ser872Arg
NM_000057.4:c.3928A>C MANE Select	NP_000048.1:p.Ser1310Arg
NM_001287246.2:c.3928A>C	NP_001274175.1:p.Ser1310Arg
NM_001287247.2:c.3535A>C	NP_001274176.1:p.Ser1179Arg
NM_001287248.2:c.2803A>C	NP_001274177.1:p.Ser935Arg