Canonical Allele Identifier: CA2195302728
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90812173C= , CM000677.2:g.90812173C= GRCh38
NC_000015.9:g.91355403C= , CM000677.1:g.91355403C= GRCh37
NC_000015.8:g.89156407C= NCBI36
NG_007272.1:g.99802C= , LRG_20:g.99802C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355112.8:c.4076+767C= MANE Select ENSP00000347232.3:n.4076+767C=
ENST00000560559.2:n.2649+767C=
ENST00000648453.1:c.*38+373C= ENSP00000497646.1:n.*38+373C=
ENST00000680772.1:c.4076+767C= ENSP00000506117.1:n.4076+767C=
ENST00000355112.7:c.4076+767C= ENSP00000347232.3:n.4076+767C=
ENST00000558825.5:n.1423+767C=
ENST00000559724.5:c.*3000+767C= ENSP00000453359.1:n.*3000+767C=
ENST00000560509.5:c.3683+767C= ENSP00000454158.1:n.3683+767C=
ENST00000560821.1:n.496+767C=
NM_000057.3:c.4076+767C= NP_000048.1:n.4076+767C=
NM_001287246.1:c.4076+767C= NP_001274175.1:n.4076+767C=
NM_001287247.1:c.3683+767C= NP_001274176.1:n.3683+767C=
NM_001287248.1:c.2951+767C= NP_001274177.1:n.2951+767C=
XM_006720632.2:c.2114+767C= XP_006720695.1:n.2114+767C=
XM_011521881.1:c.2762+767C= XP_011520183.1:n.2762+767C=
XM_011521881.2:c.2762+767C= XP_011520183.1:n.2762+767C=
NM_000057.4:c.4076+767C= MANE Select NP_000048.1:n.4076+767C=
NM_001287246.2:c.4076+767C= NP_001274175.1:n.4076+767C=
NM_001287247.2:c.3683+767C= NP_001274176.1:n.3683+767C=
NM_001287248.2:c.2951+767C= NP_001274177.1:n.2951+767C=