Canonical Allele Identifier: CA393851251
Gene: BLM HGNC NCBI

Linked Data

dbSNP Id: rs2151199912

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90811343A>G , CM000677.2:g.90811343A>G GRCh38
NC_000015.9:g.91354573A>G , CM000677.1:g.91354573A>G GRCh37
NC_000015.8:g.89155577A>G NCBI36
NG_007272.1:g.98972A>G , LRG_20:g.98972A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.4013A>G MANE Select ENSP00000347232.3:p.Lys1338Arg
ENST00000560559.2:n.2586A>G
ENST00000648453.1:c.4013A>G ENSP00000497646.1:p.Lys1338Arg
ENST00000680772.1:c.4013A>G ENSP00000506117.1:p.Lys1338Arg
ENST00000681142.1:c.4013A>G ENSP00000506682.1:p.Lys1338Arg
ENST00000355112.7:c.4013A>G ENSP00000347232.3:p.Lys1338Arg
ENST00000558825.5:n.1360A>G
ENST00000559724.5:c.*2937A>G ENSP00000453359.1:n.*2937A>G
ENST00000560509.5:c.3620A>G ENSP00000454158.1:p.Lys1207Arg
ENST00000560821.1:n.433A>G
NM_000057.3:c.4013A>G NP_000048.1:p.Lys1338Arg
NM_001287246.1:c.4013A>G NP_001274175.1:p.Lys1338Arg
NM_001287247.1:c.3620A>G NP_001274176.1:p.Lys1207Arg
NM_001287248.1:c.2888A>G NP_001274177.1:p.Lys963Arg
XM_006720632.2:c.2051A>G XP_006720695.1:p.Lys684Arg
XM_011521881.1:c.2699A>G XP_011520183.1:p.Lys900Arg
XM_011521881.2:c.2699A>G XP_011520183.1:p.Lys900Arg
NM_000057.4:c.4013A>G MANE Select NP_000048.1:p.Lys1338Arg
NM_001287246.2:c.4013A>G NP_001274175.1:p.Lys1338Arg
NM_001287247.2:c.3620A>G NP_001274176.1:p.Lys1207Arg
NM_001287248.2:c.2888A>G NP_001274177.1:p.Lys963Arg