Canonical Allele Identifier: CA2195302735
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90812192A= , CM000677.2:g.90812192A= GRCh38
NC_000015.9:g.91355422A= , CM000677.1:g.91355422A= GRCh37
NC_000015.8:g.89156426A= NCBI36
NG_007272.1:g.99821A= , LRG_20:g.99821A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.4076+786A= MANE Select ENSP00000347232.3:n.4076+786A=
ENST00000560559.2:n.2649+786A=
ENST00000648453.1:c.*38+392A= ENSP00000497646.1:n.*38+392A=
ENST00000680772.1:c.4076+786A= ENSP00000506117.1:n.4076+786A=
ENST00000355112.7:c.4076+786A= ENSP00000347232.3:n.4076+786A=
ENST00000558825.5:n.1423+786A=
ENST00000559724.5:c.*3000+786A= ENSP00000453359.1:n.*3000+786A=
ENST00000560509.5:c.3683+786A= ENSP00000454158.1:n.3683+786A=
ENST00000560821.1:n.496+786A=
NM_000057.3:c.4076+786A= NP_000048.1:n.4076+786A=
NM_001287246.1:c.4076+786A= NP_001274175.1:n.4076+786A=
NM_001287247.1:c.3683+786A= NP_001274176.1:n.3683+786A=
NM_001287248.1:c.2951+786A= NP_001274177.1:n.2951+786A=
XM_006720632.2:c.2114+786A= XP_006720695.1:n.2114+786A=
XM_011521881.1:c.2762+786A= XP_011520183.1:n.2762+786A=
XM_011521881.2:c.2762+786A= XP_011520183.1:n.2762+786A=
NM_000057.4:c.4076+786A= MANE Select NP_000048.1:n.4076+786A=
NM_001287246.2:c.4076+786A= NP_001274175.1:n.4076+786A=
NM_001287247.2:c.3683+786A= NP_001274176.1:n.3683+786A=
NM_001287248.2:c.2951+786A= NP_001274177.1:n.2951+786A=