Canonical Allele Identifier: CA2195277050
Gene: BLM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.90749579C= , CM000677.2:g.90749579C= GRCh38
NC_000015.9:g.91292809C= , CM000677.1:g.91292809C= GRCh37
NC_000015.8:g.89093813C= NCBI36
NG_007272.1:g.37208C= , LRG_20:g.37208C=

Transcript Alleles

HGVS Amino-acid Change
NM_000057.4:c.311C= MANE Select NP_000048.1:p.Ser104=
ENST00000355112.8:c.311C= MANE Select ENSP00000347232.3:p.Ser104=
NM_000057.3:c.311C= NP_000048.1:p.Ser104=
NM_001287246.1:c.311C= NP_001274175.1:p.Ser104=
NM_001287246.2:c.311C= NP_001274175.1:p.Ser104=
NM_001287247.1:c.311C= NP_001274176.1:p.Ser104=
NM_001287247.2:c.311C= NP_001274176.1:p.Ser104=
NM_001287248.1:c.-981C= NP_001274177.1:n.-981C=
NM_001287248.2:c.-981C= NP_001274177.1:n.-981C=
ENST00000355112.7:c.311C= ENSP00000347232.3:p.Ser104=
ENST00000559282.1:n.485C=
ENST00000559724.5:c.311C= ENSP00000453359.1:p.Ser104=
ENST00000560509.5:c.311C= ENSP00000454158.1:p.Ser104=
ENST00000648453.1:c.311C= ENSP00000497646.1:p.Ser104=
ENST00000680772.1:c.311C= ENSP00000506117.1:p.Ser104=
ENST00000681142.1:c.311C= ENSP00000506682.1:p.Ser104=
XM_011521882.1:c.311C= XP_011520184.1:p.Ser104=
XM_011521882.3:c.311C= XP_011520184.1:p.Ser104=