Canonical Allele Identifier: CA2195297229
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90794084T= , CM000677.2:g.90794084T= GRCh38
NC_000015.9:g.91337314T= , CM000677.1:g.91337314T= GRCh37
NC_000015.8:g.89138318T= NCBI36
NG_007272.1:g.81713T= , LRG_20:g.81713T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.3020-83T= MANE Select ENSP00000347232.3:n.3020-83T=
ENST00000560559.2:n.1593-83T=
ENST00000648453.1:c.3020-83T= ENSP00000497646.1:n.3020-83T=
ENST00000680772.1:c.3020-83T= ENSP00000506117.1:n.3020-83T=
ENST00000681142.1:c.3020-83T= ENSP00000506682.1:n.3020-83T=
ENST00000355112.7:c.3020-83T= ENSP00000347232.3:n.3020-83T=
ENST00000558825.5:n.284T=
ENST00000559724.5:c.*1944-83T= ENSP00000453359.1:n.*1944-83T=
ENST00000560136.5:n.1046-83T=
ENST00000560509.5:c.3020-83T= ENSP00000454158.1:n.3020-83T=
ENST00000560559.1:n.557-83T=
NM_000057.3:c.3020-83T= NP_000048.1:n.3020-83T=
NM_001287246.1:c.3020-83T= NP_001274175.1:n.3020-83T=
NM_001287247.1:c.3020-83T= NP_001274176.1:n.3020-83T=
NM_001287248.1:c.1895-83T= NP_001274177.1:n.1895-83T=
XM_006720632.2:c.1058-83T= XP_006720695.1:n.1058-83T=
XM_011521881.1:c.1706-83T= XP_011520183.1:n.1706-83T=
XM_011521881.2:c.1706-83T= XP_011520183.1:n.1706-83T=
NM_000057.4:c.3020-83T= MANE Select NP_000048.1:n.3020-83T=
NM_001287246.2:c.3020-83T= NP_001274175.1:n.3020-83T=
NM_001287247.2:c.3020-83T= NP_001274176.1:n.3020-83T=
NM_001287248.2:c.1895-83T= NP_001274177.1:n.1895-83T=