Canonical Allele Identifier: CA2195293685
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90804338G= , CM000677.2:g.90804338G= GRCh38
NC_000015.9:g.91347568G= , CM000677.1:g.91347568G= GRCh37
NC_000015.8:g.89148572G= NCBI36
NG_007272.1:g.91967G= , LRG_20:g.91967G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.3730G= MANE Select ENSP00000347232.3:p.Val1244=
ENST00000560559.2:n.2303G=
ENST00000648453.1:c.3730G= ENSP00000497646.1:p.Val1244=
ENST00000680772.1:c.3730G= ENSP00000506117.1:p.Val1244=
ENST00000681142.1:c.3730G= ENSP00000506682.1:p.Val1244=
ENST00000355112.7:c.3730G= ENSP00000347232.3:p.Val1244=
ENST00000558825.5:n.1077G=
ENST00000559724.5:c.*2654G= ENSP00000453359.1:n.*2654G=
ENST00000560136.5:n.1756G=
ENST00000560509.5:c.3359-4799G= ENSP00000454158.1:n.3359-4799G=
NM_000057.3:c.3730G= NP_000048.1:p.Val1244=
NM_001287246.1:c.3730G= NP_001274175.1:p.Val1244=
NM_001287247.1:c.3359-4799G= NP_001274176.1:n.3359-4799G=
NM_001287248.1:c.2605G= NP_001274177.1:p.Val869=
XM_006720632.2:c.1768G= XP_006720695.1:p.Val590=
XM_011521881.1:c.2416G= XP_011520183.1:p.Val806=
XM_011521881.2:c.2416G= XP_011520183.1:p.Val806=
NM_000057.4:c.3730G= MANE Select NP_000048.1:p.Val1244=
NM_001287246.2:c.3730G= NP_001274175.1:p.Val1244=
NM_001287247.2:c.3359-4799G= NP_001274176.1:n.3359-4799G=
NM_001287248.2:c.2605G= NP_001274177.1:p.Val869=