Canonical Allele Identifier: CA393842106
Gene: BLM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90754868A>C , CM000677.2:g.90754868A>C GRCh38
NC_000015.9:g.91298098A>C , CM000677.1:g.91298098A>C GRCh37
NC_000015.8:g.89099102A>C NCBI36
NG_007272.1:g.42497A>C , LRG_20:g.42497A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355112.8:c.1017A>C MANE Select ENSP00000347232.3:p.Lys339Asn
ENST00000648453.1:c.1017A>C ENSP00000497646.1:p.Lys339Asn
ENST00000680772.1:c.1017A>C ENSP00000506117.1:p.Lys339Asn
ENST00000681142.1:c.1017A>C ENSP00000506682.1:p.Lys339Asn
ENST00000355112.7:c.1017A>C ENSP00000347232.3:p.Lys339Asn
ENST00000558599.1:n.278A>C
ENST00000559724.5:c.1017A>C ENSP00000453359.1:p.Lys339Asn
ENST00000560509.5:c.1017A>C ENSP00000454158.1:p.Lys339Asn
NM_000057.3:c.1017A>C NP_000048.1:p.Lys339Asn
NM_001287246.1:c.1017A>C NP_001274175.1:p.Lys339Asn
NM_001287247.1:c.1017A>C NP_001274176.1:p.Lys339Asn
NM_001287248.1:c.-275A>C NP_001274177.1:n.-275A>C
XM_011521881.1:c.-165A>C XP_011520183.1:n.-165A>C
XM_011521882.1:c.1017A>C XP_011520184.1:p.Lys339Asn
XM_011521881.2:c.-165A>C XP_011520183.1:n.-165A>C
XM_011521882.3:c.1017A>C XP_011520184.1:p.Lys339Asn
NM_000057.4:c.1017A>C MANE Select NP_000048.1:p.Lys339Asn
NM_001287246.2:c.1017A>C NP_001274175.1:p.Lys339Asn
NM_001287247.2:c.1017A>C NP_001274176.1:p.Lys339Asn
NM_001287248.2:c.-275A>C NP_001274177.1:n.-275A>C