Canonical Allele Identifier: CA2195293676
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90804336C= , CM000677.2:g.90804336C= GRCh38
NC_000015.9:g.91347566C= , CM000677.1:g.91347566C= GRCh37
NC_000015.8:g.89148570C= NCBI36
NG_007272.1:g.91965C= , LRG_20:g.91965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355112.8:c.3728C= MANE Select ENSP00000347232.3:p.Thr1243=
ENST00000560559.2:n.2301C=
ENST00000648453.1:c.3728C= ENSP00000497646.1:p.Thr1243=
ENST00000680772.1:c.3728C= ENSP00000506117.1:p.Thr1243=
ENST00000681142.1:c.3728C= ENSP00000506682.1:p.Thr1243=
ENST00000355112.7:c.3728C= ENSP00000347232.3:p.Thr1243=
ENST00000558825.5:n.1075C=
ENST00000559724.5:c.*2652C= ENSP00000453359.1:n.*2652C=
ENST00000560136.5:n.1754C=
ENST00000560509.5:c.3359-4801C= ENSP00000454158.1:n.3359-4801C=
NM_000057.3:c.3728C= NP_000048.1:p.Thr1243=
NM_001287246.1:c.3728C= NP_001274175.1:p.Thr1243=
NM_001287247.1:c.3359-4801C= NP_001274176.1:n.3359-4801C=
NM_001287248.1:c.2603C= NP_001274177.1:p.Thr868=
XM_006720632.2:c.1766C= XP_006720695.1:p.Thr589=
XM_011521881.1:c.2414C= XP_011520183.1:p.Thr805=
XM_011521881.2:c.2414C= XP_011520183.1:p.Thr805=
NM_000057.4:c.3728C= MANE Select NP_000048.1:p.Thr1243=
NM_001287246.2:c.3728C= NP_001274175.1:p.Thr1243=
NM_001287247.2:c.3359-4801C= NP_001274176.1:n.3359-4801C=
NM_001287248.2:c.2603C= NP_001274177.1:p.Thr868=