Canonical Allele Identifier: CA2195302296
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90811167C= , CM000677.2:g.90811167C= GRCh38
NC_000015.9:g.91354397C= , CM000677.1:g.91354397C= GRCh37
NC_000015.8:g.89155401C= NCBI36
NG_007272.1:g.98796C= , LRG_20:g.98796C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.3875-38C= MANE Select ENSP00000347232.3:n.3875-38C=
ENST00000560559.2:n.2448-38C=
ENST00000648453.1:c.3875-38C= ENSP00000497646.1:n.3875-38C=
ENST00000680772.1:c.3875-38C= ENSP00000506117.1:n.3875-38C=
ENST00000681142.1:c.3875-38C= ENSP00000506682.1:n.3875-38C=
ENST00000355112.7:c.3875-38C= ENSP00000347232.3:n.3875-38C=
ENST00000558825.5:n.1222-38C=
ENST00000559724.5:c.*2799-38C= ENSP00000453359.1:n.*2799-38C=
ENST00000560136.5:n.1901-38C=
ENST00000560509.5:c.3482-38C= ENSP00000454158.1:n.3482-38C=
ENST00000560821.1:n.295-38C=
NM_000057.3:c.3875-38C= NP_000048.1:n.3875-38C=
NM_001287246.1:c.3875-38C= NP_001274175.1:n.3875-38C=
NM_001287247.1:c.3482-38C= NP_001274176.1:n.3482-38C=
NM_001287248.1:c.2750-38C= NP_001274177.1:n.2750-38C=
XM_006720632.2:c.1913-38C= XP_006720695.1:n.1913-38C=
XM_011521881.1:c.2561-38C= XP_011520183.1:n.2561-38C=
XM_011521881.2:c.2561-38C= XP_011520183.1:n.2561-38C=
NM_000057.4:c.3875-38C= MANE Select NP_000048.1:n.3875-38C=
NM_001287246.2:c.3875-38C= NP_001274175.1:n.3875-38C=
NM_001287247.2:c.3482-38C= NP_001274176.1:n.3482-38C=
NM_001287248.2:c.2750-38C= NP_001274177.1:n.2750-38C=