Canonical Allele Identifier: CA492157863

Gene: BLM

Linked Data

• ClinVar Variation Id: 2751097
• ClinVar RCV Id: RCV003504779
• MyVariant Identifiers: chr15:g.91354562G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811332G>A , CM000677.2:g.90811332G>A	GRCh38
NC_000015.9:g.91354562G>A , CM000677.1:g.91354562G>A	GRCh37
NC_000015.8:g.89155566G>A	NCBI36
NG_007272.1:g.98961G>A , LRG_20:g.98961G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.4002G>A MANE Select	ENSP00000347232.3:p.Arg1334=
ENST00000560559.2:n.2575G>A
ENST00000648453.1:c.4002G>A	ENSP00000497646.1:p.Arg1334=
ENST00000680772.1:c.4002G>A	ENSP00000506117.1:p.Arg1334=
ENST00000681142.1:c.4002G>A	ENSP00000506682.1:p.Arg1334=
ENST00000355112.7:c.4002G>A	ENSP00000347232.3:p.Arg1334=
ENST00000558825.5:n.1349G>A
ENST00000559724.5:c.*2926G>A	ENSP00000453359.1:n.*2926G>A
ENST00000560509.5:c.3609G>A	ENSP00000454158.1:p.Arg1203=
ENST00000560821.1:n.422G>A
NM_000057.3:c.4002G>A	NP_000048.1:p.Arg1334=
NM_001287246.1:c.4002G>A	NP_001274175.1:p.Arg1334=
NM_001287247.1:c.3609G>A	NP_001274176.1:p.Arg1203=
NM_001287248.1:c.2877G>A	NP_001274177.1:p.Arg959=
XM_006720632.2:c.2040G>A	XP_006720695.1:p.Arg680=
XM_011521881.1:c.2688G>A	XP_011520183.1:p.Arg896=
XM_011521881.2:c.2688G>A	XP_011520183.1:p.Arg896=
NM_000057.4:c.4002G>A MANE Select	NP_000048.1:p.Arg1334=
NM_001287246.2:c.4002G>A	NP_001274175.1:p.Arg1334=
NM_001287247.2:c.3609G>A	NP_001274176.1:p.Arg1203=
NM_001287248.2:c.2877G>A	NP_001274177.1:p.Arg959=