Canonical Allele Identifier: CA393848286
Gene: BLM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90804347A>G , CM000677.2:g.90804347A>G GRCh38
NC_000015.9:g.91347577A>G , CM000677.1:g.91347577A>G GRCh37
NC_000015.8:g.89148581A>G NCBI36
NG_007272.1:g.91976A>G , LRG_20:g.91976A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.3739A>G MANE Select ENSP00000347232.3:p.Lys1247Glu
ENST00000560559.2:n.2312A>G
ENST00000648453.1:c.3739A>G ENSP00000497646.1:p.Lys1247Glu
ENST00000680772.1:c.3739A>G ENSP00000506117.1:p.Lys1247Glu
ENST00000681142.1:c.3739A>G ENSP00000506682.1:p.Lys1247Glu
ENST00000355112.7:c.3739A>G ENSP00000347232.3:p.Lys1247Glu
ENST00000558825.5:n.1086A>G
ENST00000559724.5:c.*2663A>G ENSP00000453359.1:n.*2663A>G
ENST00000560136.5:n.1765A>G
ENST00000560509.5:c.3359-4790A>G ENSP00000454158.1:n.3359-4790A>G
NM_000057.3:c.3739A>G NP_000048.1:p.Lys1247Glu
NM_001287246.1:c.3739A>G NP_001274175.1:p.Lys1247Glu
NM_001287247.1:c.3359-4790A>G NP_001274176.1:n.3359-4790A>G
NM_001287248.1:c.2614A>G NP_001274177.1:p.Lys872Glu
XM_006720632.2:c.1777A>G XP_006720695.1:p.Lys593Glu
XM_011521881.1:c.2425A>G XP_011520183.1:p.Lys809Glu
XM_011521881.2:c.2425A>G XP_011520183.1:p.Lys809Glu
NM_000057.4:c.3739A>G MANE Select NP_000048.1:p.Lys1247Glu
NM_001287246.2:c.3739A>G NP_001274175.1:p.Lys1247Glu
NM_001287247.2:c.3359-4790A>G NP_001274176.1:n.3359-4790A>G
NM_001287248.2:c.2614A>G NP_001274177.1:p.Lys872Glu