Canonical Allele Identifier: CA393851488

Gene: BLM

Linked Data

• gnomAD v4: 15-90811381-G-A
• MyVariant Identifiers: chr15:g.91354611G>A (hg19) ; chr15:g.90811381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811381G>A , CM000677.2:g.90811381G>A	GRCh38
NC_000015.9:g.91354611G>A , CM000677.1:g.91354611G>A	GRCh37
NC_000015.8:g.89155615G>A	NCBI36
NG_007272.1:g.99010G>A , LRG_20:g.99010G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.4051G>A MANE Select	ENSP00000347232.3:p.Ala1351Thr
ENST00000560559.2:n.2624G>A
ENST00000648453.1:c.4051G>A	ENSP00000497646.1:p.Ala1351Thr
ENST00000680772.1:c.4051G>A	ENSP00000506117.1:p.Ala1351Thr
ENST00000681142.1:c.4051G>A	ENSP00000506682.1:p.Ala1351Thr
ENST00000355112.7:c.4051G>A	ENSP00000347232.3:p.Ala1351Thr
ENST00000558825.5:n.1398G>A
ENST00000559724.5:c.*2975G>A	ENSP00000453359.1:n.*2975G>A
ENST00000560509.5:c.3658G>A	ENSP00000454158.1:p.Ala1220Thr
ENST00000560821.1:n.471G>A
NM_000057.3:c.4051G>A	NP_000048.1:p.Ala1351Thr
NM_001287246.1:c.4051G>A	NP_001274175.1:p.Ala1351Thr
NM_001287247.1:c.3658G>A	NP_001274176.1:p.Ala1220Thr
NM_001287248.1:c.2926G>A	NP_001274177.1:p.Ala976Thr
XM_006720632.2:c.2089G>A	XP_006720695.1:p.Ala697Thr
XM_011521881.1:c.2737G>A	XP_011520183.1:p.Ala913Thr
XM_011521881.2:c.2737G>A	XP_011520183.1:p.Ala913Thr
NM_000057.4:c.4051G>A MANE Select	NP_000048.1:p.Ala1351Thr
NM_001287246.2:c.4051G>A	NP_001274175.1:p.Ala1351Thr
NM_001287247.2:c.3658G>A	NP_001274176.1:p.Ala1220Thr
NM_001287248.2:c.2926G>A	NP_001274177.1:p.Ala976Thr