Canonical Allele Identifier: CA2195280972
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90754758T= , CM000677.2:g.90754758T= GRCh38
NC_000015.9:g.91297988T= , CM000677.1:g.91297988T= GRCh37
NC_000015.8:g.89098992T= NCBI36
NG_007272.1:g.42387T= , LRG_20:g.42387T=

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.960-53T= MANE Select ENSP00000347232.3:n.960-53T=
ENST00000648453.1:c.960-53T= ENSP00000497646.1:n.960-53T=
ENST00000680772.1:c.960-53T= ENSP00000506117.1:n.960-53T=
ENST00000681142.1:c.960-53T= ENSP00000506682.1:n.960-53T=
ENST00000355112.7:c.960-53T= ENSP00000347232.3:n.960-53T=
ENST00000558599.1:n.221-53T=
ENST00000559724.5:c.960-53T= ENSP00000453359.1:n.960-53T=
ENST00000560509.5:c.960-53T= ENSP00000454158.1:n.960-53T=
NM_000057.3:c.960-53T= NP_000048.1:n.960-53T=
NM_001287246.1:c.960-53T= NP_001274175.1:n.960-53T=
NM_001287247.1:c.960-53T= NP_001274176.1:n.960-53T=
NM_001287248.1:c.-332-53T= NP_001274177.1:n.-332-53T=
XM_011521881.1:c.-222-53T= XP_011520183.1:n.-222-53T=
XM_011521882.1:c.960-53T= XP_011520184.1:n.960-53T=
XM_011521881.2:c.-222-53T= XP_011520183.1:n.-222-53T=
XM_011521882.3:c.960-53T= XP_011520184.1:n.960-53T=
NM_000057.4:c.960-53T= MANE Select NP_000048.1:n.960-53T=
NM_001287246.2:c.960-53T= NP_001274175.1:n.960-53T=
NM_001287247.2:c.960-53T= NP_001274176.1:n.960-53T=
NM_001287248.2:c.-332-53T= NP_001274177.1:n.-332-53T=