Canonical Allele Identifier: CA2195295605
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90790591A= , CM000677.2:g.90790591A= GRCh38
NC_000015.9:g.91333821A= , CM000677.1:g.91333821A= GRCh37
NC_000015.8:g.89134825A= NCBI36
NG_007272.1:g.78220A= , LRG_20:g.78220A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355112.8:c.2824-58A= MANE Select ENSP00000347232.3:n.2824-58A=
ENST00000560559.2:n.1339A=
ENST00000648453.1:c.2824-58A= ENSP00000497646.1:n.2824-58A=
ENST00000680772.1:c.2824-58A= ENSP00000506117.1:n.2824-58A=
ENST00000681142.1:c.2824-58A= ENSP00000506682.1:n.2824-58A=
ENST00000355112.7:c.2824-58A= ENSP00000347232.3:n.2824-58A=
ENST00000559724.5:c.*1748-58A= ENSP00000453359.1:n.*1748-58A=
ENST00000560136.5:n.850-58A=
ENST00000560509.5:c.2824-58A= ENSP00000454158.1:n.2824-58A=
ENST00000560559.1:n.303A=
NM_000057.3:c.2824-58A= NP_000048.1:n.2824-58A=
NM_001287246.1:c.2824-58A= NP_001274175.1:n.2824-58A=
NM_001287247.1:c.2824-58A= NP_001274176.1:n.2824-58A=
NM_001287248.1:c.1699-58A= NP_001274177.1:n.1699-58A=
XM_006720632.2:c.862-58A= XP_006720695.1:n.862-58A=
XM_011521881.1:c.1510-58A= XP_011520183.1:n.1510-58A=
XM_011521881.2:c.1510-58A= XP_011520183.1:n.1510-58A=
NM_000057.4:c.2824-58A= MANE Select NP_000048.1:n.2824-58A=
NM_001287246.2:c.2824-58A= NP_001274175.1:n.2824-58A=
NM_001287247.2:c.2824-58A= NP_001274176.1:n.2824-58A=
NM_001287248.2:c.1699-58A= NP_001274177.1:n.1699-58A=