Canonical Allele Identifier: CA393850406

Gene: BLM

Linked Data

• MyVariant Identifiers: chr15:g.91354446T>G (hg19) ; chr15:g.90811216T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.90811216T>G , CM000677.2:g.90811216T>G	GRCh38
NC_000015.9:g.91354446T>G , CM000677.1:g.91354446T>G	GRCh37
NC_000015.8:g.89155450T>G	NCBI36
NG_007272.1:g.98845T>G , LRG_20:g.98845T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355112.8:c.3886T>G MANE Select	ENSP00000347232.3:p.Ser1296Ala
ENST00000560559.2:n.2459T>G
ENST00000648453.1:c.3886T>G	ENSP00000497646.1:p.Ser1296Ala
ENST00000680772.1:c.3886T>G	ENSP00000506117.1:p.Ser1296Ala
ENST00000681142.1:c.3886T>G	ENSP00000506682.1:p.Ser1296Ala
ENST00000355112.7:c.3886T>G	ENSP00000347232.3:p.Ser1296Ala
ENST00000558825.5:n.1233T>G
ENST00000559724.5:c.*2810T>G	ENSP00000453359.1:n.*2810T>G
ENST00000560136.5:n.1912T>G
ENST00000560509.5:c.3493T>G	ENSP00000454158.1:p.Ser1165Ala
ENST00000560821.1:n.306T>G
NM_000057.3:c.3886T>G	NP_000048.1:p.Ser1296Ala
NM_001287246.1:c.3886T>G	NP_001274175.1:p.Ser1296Ala
NM_001287247.1:c.3493T>G	NP_001274176.1:p.Ser1165Ala
NM_001287248.1:c.2761T>G	NP_001274177.1:p.Ser921Ala
XM_006720632.2:c.1924T>G	XP_006720695.1:p.Ser642Ala
XM_011521881.1:c.2572T>G	XP_011520183.1:p.Ser858Ala
XM_011521881.2:c.2572T>G	XP_011520183.1:p.Ser858Ala
NM_000057.4:c.3886T>G MANE Select	NP_000048.1:p.Ser1296Ala
NM_001287246.2:c.3886T>G	NP_001274175.1:p.Ser1296Ala
NM_001287247.2:c.3493T>G	NP_001274176.1:p.Ser1165Ala
NM_001287248.2:c.2761T>G	NP_001274177.1:p.Ser921Ala